Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.153954625G>A | CA519702281 | HCFC1 | c.3774C>T (p.Cys1258=) c.3576C>T (p.Cys1192=) c.2865C>T (p.Cys955=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
X | g.153954625G>C | CA415119454 | HCFC1 | c.3774C>G (p.Cys1258Trp) c.3576C>G (p.Cys1192Trp) c.2865C>G (p.Cys955Trp) | |
X | g.153954625G= | CA2466540210 | HCFC1 | c.3774C= (p.Cys1258=) c.3576C= (p.Cys1192=) c.2865C= (p.Cys955=) | |
X | g.153954625G>T | CA415119456 | HCFC1 | c.3774C>A (p.Cys1258Ter) c.3576C>A (p.Cys1192Ter) c.2865C>A (p.Cys955Ter) | |
X | g.153954626C>A | CA415119459 | HCFC1 | c.3773G>T (p.Cys1258Phe) c.3575G>T (p.Cys1192Phe) c.2864G>T (p.Cys955Phe) | |
X | g.153954626C>G | CA415119462 | HCFC1 | c.3773G>C (p.Cys1258Ser) c.3575G>C (p.Cys1192Ser) c.2864G>C (p.Cys955Ser) | COSMIC COSMIC |
X | g.153954626C>T | CA415119463 | HCFC1 | c.3773G>A (p.Cys1258Tyr) c.3575G>A (p.Cys1192Tyr) c.2864G>A (p.Cys955Tyr) | gnomAD v4 |
X | g.153954627A>C | CA415119465 | HCFC1 | c.3772T>G (p.Cys1258Gly) c.3574T>G (p.Cys1192Gly) c.2863T>G (p.Cys955Gly) | |
X | g.153954627A>G | CA415119466 | HCFC1 | c.3772T>C (p.Cys1258Arg) c.3574T>C (p.Cys1192Arg) c.2863T>C (p.Cys955Arg) | |
X | g.153954627A>T | CA415119468 | HCFC1 | c.3772T>A (p.Cys1258Ser) c.3574T>A (p.Cys1192Ser) c.2863T>A (p.Cys955Ser) | |
X | g.153954628C>A | CA519702289 | HCFC1 | c.3771G>T (p.Val1257=) c.3573G>T (p.Val1191=) c.2862G>T (p.Val954=) | |
X | g.153954628C>G | CA519702292 | HCFC1 | c.3771G>C (p.Val1257=) c.3573G>C (p.Val1191=) c.2862G>C (p.Val954=) | |
X | g.153954628C>T | CA519702294 | HCFC1 | c.3771G>A (p.Val1257=) c.3573G>A (p.Val1191=) c.2862G>A (p.Val954=) | |
X | g.153954629A>C | CA415119471 | HCFC1 | c.3770T>G (p.Val1257Gly) c.3572T>G (p.Val1191Gly) c.2861T>G (p.Val954Gly) | |
X | g.153954629A>G | CA415119472 | HCFC1 | c.3770T>C (p.Val1257Ala) c.3572T>C (p.Val1191Ala) c.2861T>C (p.Val954Ala) | |
X | g.153954629A>T | CA415119476 | HCFC1 | c.3770T>A (p.Val1257Glu) c.3572T>A (p.Val1191Glu) c.2861T>A (p.Val954Glu) | COSMIC COSMIC |
X | g.153954630C>A | CA415119479 | HCFC1 | c.3769G>T (p.Val1257Leu) c.3571G>T (p.Val1191Leu) c.2860G>T (p.Val954Leu) | |
X | g.153954630C>G | CA415119483 | HCFC1 | c.3769G>C (p.Val1257Leu) c.3571G>C (p.Val1191Leu) c.2860G>C (p.Val954Leu) | |
X | g.153954630C>T | CA415119481 | HCFC1 | c.3769G>A (p.Val1257Met) c.3571G>A (p.Val1191Met) c.2860G>A (p.Val954Met) | |
X | g.153954631A>C | CA519702299 | HCFC1 | c.3768T>G (p.Pro1256=) c.3570T>G (p.Pro1190=) c.2859T>G (p.Pro953=) | |
X | g.153954631A>G | CA519702302 | HCFC1 | c.3768T>C (p.Pro1256=) c.3570T>C (p.Pro1190=) c.2859T>C (p.Pro953=) | gnomAD v4 |
X | g.153954631A>T | CA519702303 | HCFC1 | c.3768T>A (p.Pro1256=) c.3570T>A (p.Pro1190=) c.2859T>A (p.Pro953=) | |
X | g.153954632G>A | CA415119487 | HCFC1 | c.3767C>T (p.Pro1256Leu) c.3569C>T (p.Pro1190Leu) c.2858C>T (p.Pro953Leu) | ClinVar |
X | g.153954632G>C | CA10557131 | HCFC1 | c.3767C>G (p.Pro1256Arg) c.3569C>G (p.Pro1190Arg) c.2858C>G (p.Pro953Arg) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.153954632G= | CA2466540211 | HCFC1 | c.3767C= (p.Pro1256=) c.3569C= (p.Pro1190=) c.2858C= (p.Pro953=) | |
X | g.153954632G>T | CA415119490 | HCFC1 | c.3767C>A (p.Pro1256His) c.3569C>A (p.Pro1190His) c.2858C>A (p.Pro953His) | |
X | g.153954633G>A | CA10557132 | HCFC1 | c.3766C>T (p.Pro1256Ser) c.3568C>T (p.Pro1190Ser) c.2857C>T (p.Pro953Ser) | dbSNP ExAC gnomAD v2 gnomAD v4 |
X | g.153954633G>C | CA415119495 | HCFC1 | c.3766C>G (p.Pro1256Ala) c.3568C>G (p.Pro1190Ala) c.2857C>G (p.Pro953Ala) | |
X | g.153954633G= | CA2466540212 | HCFC1 | c.3766C= (p.Pro1256=) c.3568C= (p.Pro1190=) c.2857C= (p.Pro953=) | |
X | g.153954633G>T | CA415119497 | HCFC1 | c.3766C>A (p.Pro1256Thr) c.3568C>A (p.Pro1190Thr) c.2857C>A (p.Pro953Thr) | |
X | g.153954634T>A | CA519702310 | HCFC1 | c.3765A>T (p.Ala1255=) c.3567A>T (p.Ala1189=) c.2856A>T (p.Ala952=) | |
X | g.153954634T>C | CA519702314 | HCFC1 | c.3765A>G (p.Ala1255=) c.3567A>G (p.Ala1189=) c.2856A>G (p.Ala952=) | gnomAD v4 |
X | g.153954634T>G | CA519702312 | HCFC1 | c.3765A>C (p.Ala1255=) c.3567A>C (p.Ala1189=) c.2856A>C (p.Ala952=) | |
X | g.153954635G>A | CA415119498 | HCFC1 | c.3764C>T (p.Ala1255Val) c.3566C>T (p.Ala1189Val) c.2855C>T (p.Ala952Val) | |
X | g.153954635G>C | CA415119501 | HCFC1 | c.3764C>G (p.Ala1255Gly) c.3566C>G (p.Ala1189Gly) c.2855C>G (p.Ala952Gly) | |
X | g.153954635G>T | CA415119508 | HCFC1 | c.3764C>A (p.Ala1255Glu) c.3566C>A (p.Ala1189Glu) c.2855C>A (p.Ala952Glu) | |
X | g.153954636C>A | CA415119513 | HCFC1 | c.3763G>T (p.Ala1255Ser) c.3565G>T (p.Ala1189Ser) c.2854G>T (p.Ala952Ser) | |
X | g.153954636C>G | CA415119515 | HCFC1 | c.3763G>C (p.Ala1255Pro) c.3565G>C (p.Ala1189Pro) c.2854G>C (p.Ala952Pro) | |
X | g.153954636C>T | CA415119517 | HCFC1 | c.3763G>A (p.Ala1255Thr) c.3565G>A (p.Ala1189Thr) c.2854G>A (p.Ala952Thr) | |
X | g.153954637C>A | CA415119521 | HCFC1 | c.3762G>T (p.Met1254Ile) c.3564G>T (p.Met1188Ile) c.2853G>T (p.Met951Ile) | |
X | g.153954637C= | CA2466540213 | HCFC1 | c.3762G= (p.Met1254=) c.3564G= (p.Met1188=) c.2853G= (p.Met951=) | |
X | g.153954637C>G | CA415119523 | HCFC1 | c.3762G>C (p.Met1254Ile) c.3564G>C (p.Met1188Ile) c.2853G>C (p.Met951Ile) | |
X | g.153954637C>T | CA415119525 | HCFC1 | c.3762G>A (p.Met1254Ile) c.3564G>A (p.Met1188Ile) c.2853G>A (p.Met951Ile) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.153954638A>C | CA415119532 | HCFC1 | c.3761T>G (p.Met1254Arg) c.3563T>G (p.Met1188Arg) c.2852T>G (p.Met951Arg) | |
X | g.153954638A>G | CA415119529 | HCFC1 | c.3761T>C (p.Met1254Thr) c.3563T>C (p.Met1188Thr) c.2852T>C (p.Met951Thr) | |
X | g.153954638A>T | CA415119528 | HCFC1 | c.3761T>A (p.Met1254Lys) c.3563T>A (p.Met1188Lys) c.2852T>A (p.Met951Lys) | |
X | g.153954639T>A | CA415119534 | HCFC1 | c.3760A>T (p.Met1254Leu) c.3562A>T (p.Met1188Leu) c.2851A>T (p.Met951Leu) | |
X | g.153954639T>C | CA10557133 | HCFC1 | c.3760A>G (p.Met1254Val) c.3562A>G (p.Met1188Val) c.2851A>G (p.Met951Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.153954639T>G | CA415119538 | HCFC1 | c.3760A>C (p.Met1254Leu) c.3562A>C (p.Met1188Leu) c.2851A>C (p.Met951Leu) | |
X | g.153954639T= | CA2466540214 | HCFC1 | c.3760A= (p.Met1254=) c.3562A= (p.Met1188=) c.2851A= (p.Met951=) | |
X | g.153954640G>A | CA519702329 | HCFC1 | c.3759C>T (p.Arg1253=) c.3561C>T (p.Arg1187=) c.2850C>T (p.Arg950=) | |
X | g.153954640G>C | CA519702330 | HCFC1 | c.3759C>G (p.Arg1253=) c.3561C>G (p.Arg1187=) c.2850C>G (p.Arg950=) | |
X | g.153954640G>T | CA519702332 | HCFC1 | c.3759C>A (p.Arg1253=) c.3561C>A (p.Arg1187=) c.2850C>A (p.Arg950=) | |
X | g.153954641C>A | CA10557135 | HCFC1 | c.3758G>T (p.Arg1253Leu) c.3560G>T (p.Arg1187Leu) c.2849G>T (p.Arg950Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
X | g.153954641C= | CA2466540215 | HCFC1 | c.3758G= (p.Arg1253=) c.3560G= (p.Arg1187=) c.2849G= (p.Arg950=) | |
X | g.153954641C>G | CA10557136 | HCFC1 | c.3758G>C (p.Arg1253Pro) c.3560G>C (p.Arg1187Pro) c.2849G>C (p.Arg950Pro) | dbSNP ExAC gnomAD v2 gnomAD v4 |
X | g.153954641C>T | CA10557134 | HCFC1 | c.3758G>A (p.Arg1253His) c.3560G>A (p.Arg1187His) c.2849G>A (p.Arg950His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.153954642G>A | CA10557137 | HCFC1 | c.3757C>T (p.Arg1253Cys) c.3559C>T (p.Arg1187Cys) c.2848C>T (p.Arg950Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.153954642G>C | CA415119547 | HCFC1 | c.3757C>G (p.Arg1253Gly) c.3559C>G (p.Arg1187Gly) c.2848C>G (p.Arg950Gly) | |
X | g.153954642G= | CA2466540216 | HCFC1 | c.3757C= (p.Arg1253=) c.3559C= (p.Arg1187=) c.2848C= (p.Arg950=) | |
X | g.153954642G>T | CA415119549 | HCFC1 | c.3757C>A (p.Arg1253Ser) c.3559C>A (p.Arg1187Ser) c.2848C>A (p.Arg950Ser) | |
X | g.153954643G>A | CA519702342 | HCFC1 | c.3756C>T (p.Pro1252=) c.3558C>T (p.Pro1186=) c.2847C>T (p.Pro949=) | |
X | g.153954643G>C | CA519702341 | HCFC1 | c.3756C>G (p.Pro1252=) c.3558C>G (p.Pro1186=) c.2847C>G (p.Pro949=) | gnomAD v4 |
X | g.153954643G>T | CA519702340 | HCFC1 | c.3756C>A (p.Pro1252=) c.3558C>A (p.Pro1186=) c.2847C>A (p.Pro949=) | ClinVar gnomAD v4 |
X | g.153954644G>A | CA415119551 | HCFC1 | c.3755C>T (p.Pro1252Leu) c.3557C>T (p.Pro1186Leu) c.2846C>T (p.Pro949Leu) | |
X | g.153954644G>C | CA415119553 | HCFC1 | c.3755C>G (p.Pro1252Arg) c.3557C>G (p.Pro1186Arg) c.2846C>G (p.Pro949Arg) | dbSNP gnomAD v2 gnomAD v4 |
X | g.153954644G= | CA2466540217 | HCFC1 | c.3755C= (p.Pro1252=) c.3557C= (p.Pro1186=) c.2846C= (p.Pro949=) | |
X | g.153954644G>T | CA415119556 | HCFC1 | c.3755C>A (p.Pro1252His) c.3557C>A (p.Pro1186His) c.2846C>A (p.Pro949His) | |
X | g.153954645G>A | CA10557138 | HCFC1 | c.3754C>T (p.Pro1252Ser) c.3556C>T (p.Pro1186Ser) c.2845C>T (p.Pro949Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.153954645G>C | CA415119562 | HCFC1 | c.3754C>G (p.Pro1252Ala) c.3556C>G (p.Pro1186Ala) c.2845C>G (p.Pro949Ala) | |
X | g.153954645G= | CA2466540218 | HCFC1 | c.3754C= (p.Pro1252=) c.3556C= (p.Pro1186=) c.2845C= (p.Pro949=) | |
X | g.153954645G>T | CA415119561 | HCFC1 | c.3754C>A (p.Pro1252Thr) c.3556C>A (p.Pro1186Thr) c.2845C>A (p.Pro949Thr) | |
X | g.153954646C>A | CA415119564 | HCFC1 | c.3753G>T (p.Glu1251Asp) c.3555G>T (p.Glu1185Asp) c.2844G>T (p.Glu948Asp) | |
X | g.153954646C>G | CA415119566 | HCFC1 | c.3753G>C (p.Glu1251Asp) c.3555G>C (p.Glu1185Asp) c.2844G>C (p.Glu948Asp) | |
X | g.153954646C>T | CA519702349 | HCFC1 | c.3753G>A (p.Glu1251=) c.3555G>A (p.Glu1185=) c.2844G>A (p.Glu948=) | |
X | g.153954647T>A | CA415119569 | HCFC1 | c.3752A>T (p.Glu1251Val) c.3554A>T (p.Glu1185Val) c.2843A>T (p.Glu948Val) | |
X | g.153954647T>C | CA415119571 | HCFC1 | c.3752A>G (p.Glu1251Gly) c.3554A>G (p.Glu1185Gly) c.2843A>G (p.Glu948Gly) | ClinVar |
X | g.153954647T>G | CA415119572 | HCFC1 | c.3752A>C (p.Glu1251Ala) c.3554A>C (p.Glu1185Ala) c.2843A>C (p.Glu948Ala) | |
X | g.153954648C>A | CA415119575 | HCFC1 | c.3751G>T (p.Glu1251Ter) c.3553G>T (p.Glu1185Ter) c.2842G>T (p.Glu948Ter) | |
X | g.153954648C>G | CA415119577 | HCFC1 | c.3751G>C (p.Glu1251Gln) c.3553G>C (p.Glu1185Gln) c.2842G>C (p.Glu948Gln) | |
X | g.153954648C>T | CA415119579 | HCFC1 | c.3751G>A (p.Glu1251Lys) c.3553G>A (p.Glu1185Lys) c.2842G>A (p.Glu948Lys) | |
X | g.153954651del | CA2579735262 | HCFC1 | c.3751del (p.Glu1251SerfsTer20) c.3553del (p.Glu1185SerfsTer20) c.2842del (p.Glu948SerfsTer20) | |
X | g.153954649C>A | CA519702354 | HCFC1 | c.3750G>T (p.Gly1250=) c.3552G>T (p.Gly1184=) c.2841G>T (p.Gly947=) | |
X | g.153954649C>G | CA519702357 | HCFC1 | c.3750G>C (p.Gly1250=) c.3552G>C (p.Gly1184=) c.2841G>C (p.Gly947=) | |
X | g.153954649C>T | CA519702359 | HCFC1 | c.3750G>A (p.Gly1250=) c.3552G>A (p.Gly1184=) c.2841G>A (p.Gly947=) | |
X | g.153954650C>A | CA415119581 | HCFC1 | c.3749G>T (p.Gly1250Val) c.3551G>T (p.Gly1184Val) c.2840G>T (p.Gly947Val) | gnomAD v4 |
X | g.153954650C= | CA2466540219 | HCFC1 | c.3749G= (p.Gly1250=) c.3551G= (p.Gly1184=) c.2840G= (p.Gly947=) | |
X | g.153954650C>G | CA415119582 | HCFC1 | c.3749G>C (p.Gly1250Ala) c.3551G>C (p.Gly1184Ala) c.2840G>C (p.Gly947Ala) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.153954650C>T | CA415119584 | HCFC1 | c.3749G>A (p.Gly1250Glu) c.3551G>A (p.Gly1184Glu) c.2840G>A (p.Gly947Glu) | |
X | g.153954651C>A | CA415119591 | HCFC1 | c.3748G>T (p.Gly1250Trp) c.3550G>T (p.Gly1184Trp) c.2839G>T (p.Gly947Trp) | |
X | g.153954651C= | CA2466540220 | HCFC1 | c.3748G= (p.Gly1250=) c.3550G= (p.Gly1184=) c.2839G= (p.Gly947=) | |
X | g.153954651C>G | CA415119589 | HCFC1 | c.3748G>C (p.Gly1250Arg) c.3550G>C (p.Gly1184Arg) c.2839G>C (p.Gly947Arg) | |
X | g.153954651C>T | CA337252709 | HCFC1 | c.3748G>A (p.Gly1250Arg) c.3550G>A (p.Gly1184Arg) c.2839G>A (p.Gly947Arg) | dbSNP |
X | g.153954652A>C | CA519702366 | HCFC1 | c.3747T>G (p.Ala1249=) c.3549T>G (p.Ala1183=) c.2838T>G (p.Ala946=) | |
X | g.153954652A>G | CA519702368 | HCFC1 | c.3747T>C (p.Ala1249=) c.3549T>C (p.Ala1183=) c.2838T>C (p.Ala946=) | |
X | g.153954652A>T | CA519702369 | HCFC1 | c.3747T>A (p.Ala1249=) c.3549T>A (p.Ala1183=) c.2838T>A (p.Ala946=) | |
X | g.153954653G>A | CA415119594 | HCFC1 | c.3746C>T (p.Ala1249Val) c.3548C>T (p.Ala1183Val) c.2837C>T (p.Ala946Val) | |
X | g.153954653G>C | CA415119597 | HCFC1 | c.3746C>G (p.Ala1249Gly) c.3548C>G (p.Ala1183Gly) c.2837C>G (p.Ala946Gly) | |
X | g.153954653G>T | CA415119599 | HCFC1 | c.3746C>A (p.Ala1249Asp) c.3548C>A (p.Ala1183Asp) c.2837C>A (p.Ala946Asp) | |
X | g.153954654C>A | CA415119601 | HCFC1 | c.3745G>T (p.Ala1249Ser) c.3547G>T (p.Ala1183Ser) c.2836G>T (p.Ala946Ser) | |
X | g.153954654C>G | CA415119604 | HCFC1 | c.3745G>C (p.Ala1249Pro) c.3547G>C (p.Ala1183Pro) c.2836G>C (p.Ala946Pro) | |
X | g.153954654C>T | CA415119607 | HCFC1 | c.3745G>A (p.Ala1249Thr) c.3547G>A (p.Ala1183Thr) c.2836G>A (p.Ala946Thr) | gnomAD v4 |
X | g.153954655A>C | CA519702378 | HCFC1 | c.3744T>G (p.Gly1248=) c.3546T>G (p.Gly1182=) c.2835T>G (p.Gly945=) | |
X | g.153954655A>G | CA519702380 | HCFC1 | c.3744T>C (p.Gly1248=) c.3546T>C (p.Gly1182=) c.2835T>C (p.Gly945=) | |
X | g.153954655A>T | CA519702381 | HCFC1 | c.3744T>A (p.Gly1248=) c.3546T>A (p.Gly1182=) c.2835T>A (p.Gly945=) | ClinVar |
X | g.153954656C>A | CA415119608 | HCFC1 | c.3743G>T (p.Gly1248Val) c.3545G>T (p.Gly1182Val) c.2834G>T (p.Gly945Val) | |
X | g.153954656C= | CA2466540221 | HCFC1 | c.3743G= (p.Gly1248=) c.3545G= (p.Gly1182=) c.2834G= (p.Gly945=) | |
X | g.153954656C>G | CA415119610 | HCFC1 | c.3743G>C (p.Gly1248Ala) c.3545G>C (p.Gly1182Ala) c.2834G>C (p.Gly945Ala) | |
X | g.153954656C>T | CA415119613 | HCFC1 | c.3743G>A (p.Gly1248Asp) c.3545G>A (p.Gly1182Asp) c.2834G>A (p.Gly945Asp) | dbSNP |
X | g.153954657C>A | CA415119621 | HCFC1 | c.3742G>T (p.Gly1248Cys) c.3544G>T (p.Gly1182Cys) c.2833G>T (p.Gly945Cys) | gnomAD v4 COSMIC COSMIC |
X | g.153954657C>G | CA415119618 | HCFC1 | c.3742G>C (p.Gly1248Arg) c.3544G>C (p.Gly1182Arg) c.2833G>C (p.Gly945Arg) | |
X | g.153954657C>T | CA415119616 | HCFC1 | c.3742G>A (p.Gly1248Ser) c.3544G>A (p.Gly1182Ser) c.2833G>A (p.Gly945Ser) | |
X | g.153954658C>A | CA519702394 | HCFC1 | c.3741G>T (p.Val1247=) c.3543G>T (p.Val1181=) c.2832G>T (p.Val944=) | |
X | g.153954658C>G | CA519702390 | HCFC1 | c.3741G>C (p.Val1247=) c.3543G>C (p.Val1181=) c.2832G>C (p.Val944=) | |
X | g.153954658C>T | CA519702388 | HCFC1 | c.3741G>A (p.Val1247=) c.3543G>A (p.Val1181=) c.2832G>A (p.Val944=) | |
X | g.153954659A>C | CA415119624 | HCFC1 | c.3740T>G (p.Val1247Gly) c.3542T>G (p.Val1181Gly) c.2831T>G (p.Val944Gly) | |
X | g.153954659A>G | CA415119628 | HCFC1 | c.3740T>C (p.Val1247Ala) c.3542T>C (p.Val1181Ala) c.2831T>C (p.Val944Ala) | |
X | g.153954659A>T | CA415119627 | HCFC1 | c.3740T>A (p.Val1247Glu) c.3542T>A (p.Val1181Glu) c.2831T>A (p.Val944Glu) | |
X | g.153954660C>A | CA415119632 | HCFC1 | c.3739G>T (p.Val1247Leu) c.3541G>T (p.Val1181Leu) c.2830G>T (p.Val944Leu) | |
X | g.153954660C= | CA2466540222 | HCFC1 | c.3739G= (p.Val1247=) c.3541G= (p.Val1181=) c.2830G= (p.Val944=) | |
X | g.153954660C>G | CA415119634 | HCFC1 | c.3739G>C (p.Val1247Leu) c.3541G>C (p.Val1181Leu) c.2830G>C (p.Val944Leu) | |
X | g.153954660C>T | CA415119636 | HCFC1 | c.3739G>A (p.Val1247Met) c.3541G>A (p.Val1181Met) c.2830G>A (p.Val944Met) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.153954661G>A | CA10557139 | HCFC1 | c.3738C>T (p.Ser1246=) c.3540C>T (p.Ser1180=) c.2829C>T (p.Ser943=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
X | g.153954661G>C | CA415119640 | HCFC1 | c.3738C>G (p.Ser1246Arg) c.3540C>G (p.Ser1180Arg) c.2829C>G (p.Ser943Arg) | |
X | g.153954661G= | CA2466540223 | HCFC1 | c.3738C= (p.Ser1246=) c.3540C= (p.Ser1180=) c.2829C= (p.Ser943=) | |
X | g.153954661G>T | CA415119643 | HCFC1 | c.3738C>A (p.Ser1246Arg) c.3540C>A (p.Ser1180Arg) c.2829C>A (p.Ser943Arg) | |
X | g.153954662C>A | CA415119647 | HCFC1 | c.3737G>T (p.Ser1246Ile) c.3539G>T (p.Ser1180Ile) c.2828G>T (p.Ser943Ile) | |
X | g.153954662C= | CA2466540224 | HCFC1 | c.3737G= (p.Ser1246=) c.3539G= (p.Ser1180=) c.2828G= (p.Ser943=) | |
X | g.153954662C>G | CA415119649 | HCFC1 | c.3737G>C (p.Ser1246Thr) c.3539G>C (p.Ser1180Thr) c.2828G>C (p.Ser943Thr) | |
X | g.153954662C>T | CA415119651 | HCFC1 | c.3737G>A (p.Ser1246Asn) c.3539G>A (p.Ser1180Asn) c.2828G>A (p.Ser943Asn) | dbSNP gnomAD v2 |
X | g.153954663T>A | CA415119655 | HCFC1 | c.3736A>T (p.Ser1246Cys) c.3538A>T (p.Ser1180Cys) c.2827A>T (p.Ser943Cys) | |
X | g.153954663T>C | CA415119657 | HCFC1 | c.3736A>G (p.Ser1246Gly) c.3538A>G (p.Ser1180Gly) c.2827A>G (p.Ser943Gly) | gnomAD v4 |
X | g.153954663T>G | CA415119659 | HCFC1 | c.3736A>C (p.Ser1246Arg) c.3538A>C (p.Ser1180Arg) c.2827A>C (p.Ser943Arg) | |
X | g.153954664G>A | CA519702406 | HCFC1 | c.3735C>T (p.Ser1245=) c.3537C>T (p.Ser1179=) c.2826C>T (p.Ser942=) | dbSNP |
X | g.153954664G>C | CA519702409 | HCFC1 | c.3735C>G (p.Ser1245=) c.3537C>G (p.Ser1179=) c.2826C>G (p.Ser942=) | |
X | g.153954664G= | CA2466540225 | HCFC1 | c.3735C= (p.Ser1245=) c.3537C= (p.Ser1179=) c.2826C= (p.Ser942=) | |
X | g.153954664G>T | CA519702410 | HCFC1 | c.3735C>A (p.Ser1245=) c.3537C>A (p.Ser1179=) c.2826C>A (p.Ser942=) | |
X | g.153954665G>A | CA10557141 | HCFC1 | c.3734C>T (p.Ser1245Phe) c.3536C>T (p.Ser1179Phe) c.2825C>T (p.Ser942Phe) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.153954665G>C | CA10557140 | HCFC1 | c.3734C>G (p.Ser1245Cys) c.3536C>G (p.Ser1179Cys) c.2825C>G (p.Ser942Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.153954665G= | CA2466540226 | HCFC1 | c.3734C= (p.Ser1245=) c.3536C= (p.Ser1179=) c.2825C= (p.Ser942=) | |
X | g.153954665G>T | CA415119664 | HCFC1 | c.3734C>A (p.Ser1245Tyr) c.3536C>A (p.Ser1179Tyr) c.2825C>A (p.Ser942Tyr) | gnomAD v4 |
X | g.153954666A>C | CA415119667 | HCFC1 | c.3733T>G (p.Ser1245Ala) c.3535T>G (p.Ser1179Ala) c.2824T>G (p.Ser942Ala) | |
X | g.153954666A>G | CA415119670 | HCFC1 | c.3733T>C (p.Ser1245Pro) c.3535T>C (p.Ser1179Pro) c.2824T>C (p.Ser942Pro) | |
X | g.153954666A>T | CA415119673 | HCFC1 | c.3733T>A (p.Ser1245Thr) c.3535T>A (p.Ser1179Thr) c.2824T>A (p.Ser942Thr) | |
X | g.153954667A>C | CA519702413 | HCFC1 | c.3732T>G (p.Arg1244=) c.3534T>G (p.Arg1178=) c.2823T>G (p.Arg941=) | |
X | g.153954667A>G | CA519702414 | HCFC1 | c.3732T>C (p.Arg1244=) c.3534T>C (p.Arg1178=) c.2823T>C (p.Arg941=) | ClinVar |
X | g.153954667A>T | CA519702417 | HCFC1 | c.3732T>A (p.Arg1244=) c.3534T>A (p.Arg1178=) c.2823T>A (p.Arg941=) | |
X | g.153954668C>A | CA415119674 | HCFC1 | c.3731G>T (p.Arg1244Leu) c.3533G>T (p.Arg1178Leu) c.2822G>T (p.Arg941Leu) | |
X | g.153954668C= | CA2466540227 | HCFC1 | c.3731G= (p.Arg1244=) c.3533G= (p.Arg1178=) c.2822G= (p.Arg941=) | |
X | g.153954668C>G | CA415119675 | HCFC1 | c.3731G>C (p.Arg1244Pro) c.3533G>C (p.Arg1178Pro) c.2822G>C (p.Arg941Pro) | dbSNP gnomAD v2 gnomAD v4 |
X | g.153954668C>T | CA10557142 | HCFC1 | c.3731G>A (p.Arg1244His) c.3533G>A (p.Arg1178His) c.2822G>A (p.Arg941His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.153954669G>A | CA10557143 | HCFC1 | c.3730C>T (p.Arg1244Cys) c.3532C>T (p.Arg1178Cys) c.2821C>T (p.Arg941Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.153954669G>C | CA415119677 | HCFC1 | c.3730C>G (p.Arg1244Gly) c.3532C>G (p.Arg1178Gly) c.2821C>G (p.Arg941Gly) | |
X | g.153954669G= | CA2466540228 | HCFC1 | c.3730C= (p.Arg1244=) c.3532C= (p.Arg1178=) c.2821C= (p.Arg941=) | |
X | g.153954669G>T | CA415119680 | HCFC1 | c.3730C>A (p.Arg1244Ser) c.3532C>A (p.Arg1178Ser) c.2821C>A (p.Arg941Ser) | |
X | g.153954670G>A | CA519702424 | HCFC1 | c.3729C>T (p.Thr1243=) c.3531C>T (p.Thr1177=) c.2820C>T (p.Thr940=) | |
X | g.153954670G>C | CA519702427 | HCFC1 | c.3729C>G (p.Thr1243=) c.3531C>G (p.Thr1177=) c.2820C>G (p.Thr940=) | gnomAD v4 |
X | g.153954670G>T | CA519702428 | HCFC1 | c.3729C>A (p.Thr1243=) c.3531C>A (p.Thr1177=) c.2820C>A (p.Thr940=) | gnomAD v4 |
X | g.153954671G>A | CA415119687 | HCFC1 | c.3728C>T (p.Thr1243Ile) c.3530C>T (p.Thr1177Ile) c.2819C>T (p.Thr940Ile) | |
X | g.153954671G>C | CA415119684 | HCFC1 | c.3728C>G (p.Thr1243Ser) c.3530C>G (p.Thr1177Ser) c.2819C>G (p.Thr940Ser) | |
X | g.153954671G>T | CA415119682 | HCFC1 | c.3728C>A (p.Thr1243Asn) c.3530C>A (p.Thr1177Asn) c.2819C>A (p.Thr940Asn) | |
X | g.153954672T>A | CA415119690 | HCFC1 | c.3727A>T (p.Thr1243Ser) c.3529A>T (p.Thr1177Ser) c.2818A>T (p.Thr940Ser) | |
X | g.153954672T>C | CA415119692 | HCFC1 | c.3727A>G (p.Thr1243Ala) c.3529A>G (p.Thr1177Ala) c.2818A>G (p.Thr940Ala) | |
X | g.153954672T>G | CA415119694 | HCFC1 | c.3727A>C (p.Thr1243Pro) c.3529A>C (p.Thr1177Pro) c.2818A>C (p.Thr940Pro) | |
X | g.153954673C>A | CA415119697 | HCFC1 | c.3726G>T (p.Met1242Ile) c.3528G>T (p.Met1176Ile) c.2817G>T (p.Met939Ile) | |
X | g.153954673C>G | CA415119699 | HCFC1 | c.3726G>C (p.Met1242Ile) c.3528G>C (p.Met1176Ile) c.2817G>C (p.Met939Ile) | |
X | g.153954673C>T | CA415119702 | HCFC1 | c.3726G>A (p.Met1242Ile) c.3528G>A (p.Met1176Ile) c.2817G>A (p.Met939Ile) | |
X | g.153954674A= | CA2466540229 | HCFC1 | c.3725T= (p.Met1242=) c.3527T= (p.Met1176=) c.2816T= (p.Met939=) | |
X | g.153954674A>C | CA415119705 | HCFC1 | c.3725T>G (p.Met1242Arg) c.3527T>G (p.Met1176Arg) c.2816T>G (p.Met939Arg) | |
X | g.153954674A>G | CA415119709 | HCFC1 | c.3725T>C (p.Met1242Thr) c.3527T>C (p.Met1176Thr) c.2816T>C (p.Met939Thr) | dbSNP gnomAD v2 gnomAD v4 |
X | g.153954674A>T | CA415119710 | HCFC1 | c.3725T>A (p.Met1242Lys) c.3527T>A (p.Met1176Lys) c.2816T>A (p.Met939Lys) | |
X | g.153954675T>A | CA415119712 | HCFC1 | c.3724A>T (p.Met1242Leu) c.3526A>T (p.Met1176Leu) c.2815A>T (p.Met939Leu) | |
X | g.153954675T>C | CA415119715 | HCFC1 | c.3724A>G (p.Met1242Val) c.3526A>G (p.Met1176Val) c.2815A>G (p.Met939Val) | dbSNP |
X | g.153954675T>G | CA415119716 | HCFC1 | c.3724A>C (p.Met1242Leu) c.3526A>C (p.Met1176Leu) c.2815A>C (p.Met939Leu) | |
X | g.153954675T= | CA2466540230 | HCFC1 | c.3724A= (p.Met1242=) c.3526A= (p.Met1176=) c.2815A= (p.Met939=) | |
X | g.153954676G>A | CA519702434 | HCFC1 | c.3723C>T (p.Ala1241=) c.3525C>T (p.Ala1175=) c.2814C>T (p.Ala938=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.153954676G>C | CA519702440 | HCFC1 | c.3723C>G (p.Ala1241=) c.3525C>G (p.Ala1175=) c.2814C>G (p.Ala938=) | |
X | g.153954676G= | CA2466540231 | HCFC1 | c.3723C= (p.Ala1241=) c.3525C= (p.Ala1175=) c.2814C= (p.Ala938=) | |
X | g.153954676G>T | CA519702437 | HCFC1 | c.3723C>A (p.Ala1241=) c.3525C>A (p.Ala1175=) c.2814C>A (p.Ala938=) | |
X | g.153954677G>A | CA415119721 | HCFC1 | c.3722C>T (p.Ala1241Val) c.3524C>T (p.Ala1175Val) c.2813C>T (p.Ala938Val) | |
X | g.153954677G>C | CA415119718 | HCFC1 | c.3722C>G (p.Ala1241Gly) c.3524C>G (p.Ala1175Gly) c.2813C>G (p.Ala938Gly) | |
X | g.153954677G>T | CA415119719 | HCFC1 | c.3722C>A (p.Ala1241Asp) c.3524C>A (p.Ala1175Asp) c.2813C>A (p.Ala938Asp) | gnomAD v4 |
X | g.153954678C>A | CA415119723 | HCFC1 | c.3721G>T (p.Ala1241Ser) c.3523G>T (p.Ala1175Ser) c.2812G>T (p.Ala938Ser) | |
X | g.153954678C>G | CA415119726 | HCFC1 | c.3721G>C (p.Ala1241Pro) c.3523G>C (p.Ala1175Pro) c.2812G>C (p.Ala938Pro) | |
X | g.153954678C>T | CA415119728 | HCFC1 | c.3721G>A (p.Ala1241Thr) c.3523G>A (p.Ala1175Thr) c.2812G>A (p.Ala938Thr) | |
X | g.153954679A>C | CA519702446 | HCFC1 | c.3720T>G (p.Ala1240=) c.3522T>G (p.Ala1174=) c.2811T>G (p.Ala937=) | |
X | g.153954679A>G | CA519702449 | HCFC1 | c.3720T>C (p.Ala1240=) c.3522T>C (p.Ala1174=) c.2811T>C (p.Ala937=) | gnomAD v4 |
X | g.153954679A>T | CA519702450 | HCFC1 | c.3720T>A (p.Ala1240=) c.3522T>A (p.Ala1174=) c.2811T>A (p.Ala937=) | |
X | g.153954680G>A | CA10557144 | HCFC1 | c.3719C>T (p.Ala1240Val) c.3521C>T (p.Ala1174Val) c.2810C>T (p.Ala937Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.153954680G>C | CA10557145 | HCFC1 | c.3719C>G (p.Ala1240Gly) c.3521C>G (p.Ala1174Gly) c.2810C>G (p.Ala937Gly) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.153954680G= | CA2466540232 | HCFC1 | c.3719C= (p.Ala1240=) c.3521C= (p.Ala1174=) c.2810C= (p.Ala937=) | |
X | g.153954680G>T | CA415119733 | HCFC1 | c.3719C>A (p.Ala1240Asp) c.3521C>A (p.Ala1174Asp) c.2810C>A (p.Ala937Asp) | gnomAD v4 |
X | g.153954681C>A | CA415119736 | HCFC1 | c.3718G>T (p.Ala1240Ser) c.3520G>T (p.Ala1174Ser) c.2809G>T (p.Ala937Ser) | |
X | g.153954681C= | CA2466540233 | HCFC1 | c.3718G= (p.Ala1240=) c.3520G= (p.Ala1174=) c.2809G= (p.Ala937=) | |
X | g.153954681C>G | CA415119739 | HCFC1 | c.3718G>C (p.Ala1240Pro) c.3520G>C (p.Ala1174Pro) c.2809G>C (p.Ala937Pro) | |
X | g.153954681C>T | CA10557146 | HCFC1 | c.3718G>A (p.Ala1240Thr) c.3520G>A (p.Ala1174Thr) c.2809G>A (p.Ala937Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.153954682G>A | CA10557147 | HCFC1 | c.3717C>T (p.Thr1239=) c.3519C>T (p.Thr1173=) c.2808C>T (p.Thr936=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
X | g.153954682G>C | CA519702455 | HCFC1 | c.3717C>G (p.Thr1239=) c.3519C>G (p.Thr1173=) c.2808C>G (p.Thr936=) | |
X | g.153954682G= | CA2466540234 | HCFC1 | c.3717C= (p.Thr1239=) c.3519C= (p.Thr1173=) c.2808C= (p.Thr936=) | |
X | g.153954682G>T | CA519702456 | HCFC1 | c.3717C>A (p.Thr1239=) c.3519C>A (p.Thr1173=) c.2808C>A (p.Thr936=) | |
X | g.153954683G>A | CA415119747 | HCFC1 | c.3716C>T (p.Thr1239Ile) c.3518C>T (p.Thr1173Ile) c.2807C>T (p.Thr936Ile) | gnomAD v4 |
X | g.153954683G>C | CA415119752 | HCFC1 | c.3716C>G (p.Thr1239Ser) c.3518C>G (p.Thr1173Ser) c.2807C>G (p.Thr936Ser) | |
X | g.153954683G>T | CA415119750 | HCFC1 | c.3716C>A (p.Thr1239Asn) c.3518C>A (p.Thr1173Asn) c.2807C>A (p.Thr936Asn) | gnomAD v4 |
X | g.153954684T>A | CA415119756 | HCFC1 | c.3715A>T (p.Thr1239Ser) c.3517A>T (p.Thr1173Ser) c.2806A>T (p.Thr936Ser) | |
X | g.153954684T>C | CA415119761 | HCFC1 | c.3715A>G (p.Thr1239Ala) c.3517A>G (p.Thr1173Ala) c.2806A>G (p.Thr936Ala) | gnomAD v4 |
X | g.153954684T>G | CA415119759 | HCFC1 | c.3715A>C (p.Thr1239Pro) c.3517A>C (p.Thr1173Pro) c.2806A>C (p.Thr936Pro) | |
X | g.153954685G>A | CA519702462 | HCFC1 | c.3714C>T (p.Ser1238=) c.3516C>T (p.Ser1172=) c.2805C>T (p.Ser935=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
X | g.153954685G>C | CA415119763 | HCFC1 | c.3714C>G (p.Ser1238Arg) c.3516C>G (p.Ser1172Arg) c.2805C>G (p.Ser935Arg) | |
X | g.153954685G= | CA2466540235 | HCFC1 | c.3714C= (p.Ser1238=) c.3516C= (p.Ser1172=) c.2805C= (p.Ser935=) | |
X | g.153954685G>T | CA415119765 | HCFC1 | c.3714C>A (p.Ser1238Arg) c.3516C>A (p.Ser1172Arg) c.2805C>A (p.Ser935Arg) | |
X | g.153954686C>A | CA415119766 | HCFC1 | c.3713G>T (p.Ser1238Ile) c.3515G>T (p.Ser1172Ile) c.2804G>T (p.Ser935Ile) | gnomAD v4 |
X | g.153954686C= | CA2466540236 | HCFC1 | c.3713G= (p.Ser1238=) c.3515G= (p.Ser1172=) c.2804G= (p.Ser935=) | |
X | g.153954686C>G | CA415119767 | HCFC1 | c.3713G>C (p.Ser1238Thr) c.3515G>C (p.Ser1172Thr) c.2804G>C (p.Ser935Thr) | |
X | g.153954686C>T | CA415119769 | HCFC1 | c.3713G>A (p.Ser1238Asn) c.3515G>A (p.Ser1172Asn) c.2804G>A (p.Ser935Asn) | dbSNP |
X | g.153954687T>A | CA415119771 | HCFC1 | c.3712A>T (p.Ser1238Cys) c.3514A>T (p.Ser1172Cys) c.2803A>T (p.Ser935Cys) | |
X | g.153954687T>C | CA415119773 | HCFC1 | c.3712A>G (p.Ser1238Gly) c.3514A>G (p.Ser1172Gly) c.2803A>G (p.Ser935Gly) | dbSNP gnomAD v3 gnomAD v4 |
X | g.153954687T>G | CA415119774 | HCFC1 | c.3712A>C (p.Ser1238Arg) c.3514A>C (p.Ser1172Arg) c.2803A>C (p.Ser935Arg) | |
X | g.153954687T= | CA2466540237 | HCFC1 | c.3712A= (p.Ser1238=) c.3514A= (p.Ser1172=) c.2803A= (p.Ser935=) | |
X | g.153954688G>A | CA10557148 | HCFC1 | c.3711C>T (p.Val1237=) c.3513C>T (p.Val1171=) c.2802C>T (p.Val934=) | dbSNP ExAC gnomAD v2 |
X | g.153954688G>C | CA519702468 | HCFC1 | c.3711C>G (p.Val1237=) c.3513C>G (p.Val1171=) c.2802C>G (p.Val934=) | |
X | g.153954688G= | CA2466540238 | HCFC1 | c.3711C= (p.Val1237=) c.3513C= (p.Val1171=) c.2802C= (p.Val934=) | |
X | g.153954688G>T | CA519702469 | HCFC1 | c.3711C>A (p.Val1237=) c.3513C>A (p.Val1171=) c.2802C>A (p.Val934=) | |
X | g.153954689A= | CA2466540239 | HCFC1 | c.3710T= (p.Val1237=) c.3512T= (p.Val1171=) c.2801T= (p.Val934=) | |
X | g.153954689A>C | CA415119775 | HCFC1 | c.3710T>G (p.Val1237Gly) c.3512T>G (p.Val1171Gly) c.2801T>G (p.Val934Gly) | |
X | g.153954689A>G | CA415119777 | HCFC1 | c.3710T>C (p.Val1237Ala) c.3512T>C (p.Val1171Ala) c.2801T>C (p.Val934Ala) | |
X | g.153954689A>T | CA10557149 | HCFC1 | c.3710T>A (p.Val1237Asp) c.3512T>A (p.Val1171Asp) c.2801T>A (p.Val934Asp) | dbSNP ExAC gnomAD v2 gnomAD v4 |
X | g.153954690C>A | CA415119782 | HCFC1 | c.3709G>T (p.Val1237Phe) c.3511G>T (p.Val1171Phe) c.2800G>T (p.Val934Phe) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.153954690C= | CA2466540240 | HCFC1 | c.3709G= (p.Val1237=) c.3511G= (p.Val1171=) c.2800G= (p.Val934=) | |
X | g.153954690C>G | CA415119780 | HCFC1 | c.3709G>C (p.Val1237Leu) c.3511G>C (p.Val1171Leu) c.2800G>C (p.Val934Leu) | |
X | g.153954690C>T | CA415119779 | HCFC1 | c.3709G>A (p.Val1237Ile) c.3511G>A (p.Val1171Ile) c.2800G>A (p.Val934Ile) | |
X | g.153954691C>A | CA519702476 | HCFC1 | c.3708G>T (p.Ala1236=) c.3510G>T (p.Ala1170=) c.2799G>T (p.Ala933=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
X | g.153954691C= | CA2466540241 | HCFC1 | c.3708G= (p.Ala1236=) c.3510G= (p.Ala1170=) c.2799G= (p.Ala933=) | |
X | g.153954691C>G | CA519702478 | HCFC1 | c.3708G>C (p.Ala1236=) c.3510G>C (p.Ala1170=) c.2799G>C (p.Ala933=) | ClinVar gnomAD v4 |
X | g.153954691C>T | CA10557150 | HCFC1 | c.3708G>A (p.Ala1236=) c.3510G>A (p.Ala1170=) c.2799G>A (p.Ala933=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.153954692G>A | CA10557151 | HCFC1 | c.3707C>T (p.Ala1236Val) c.3509C>T (p.Ala1170Val) c.2798C>T (p.Ala933Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.153954692G>C | CA415119785 | HCFC1 | c.3707C>G (p.Ala1236Gly) c.3509C>G (p.Ala1170Gly) c.2798C>G (p.Ala933Gly) | dbSNP gnomAD v2 gnomAD v4 |
X | g.153954692G= | CA2466540242 | HCFC1 | c.3707C= (p.Ala1236=) c.3509C= (p.Ala1170=) c.2798C= (p.Ala933=) | |
X | g.153954692G>T | CA415119786 | HCFC1 | c.3707C>A (p.Ala1236Glu) c.3509C>A (p.Ala1170Glu) c.2798C>A (p.Ala933Glu) | gnomAD v4 |
X | g.153954693C>A | CA415119788 | HCFC1 | c.3706G>T (p.Ala1236Ser) c.3508G>T (p.Ala1170Ser) c.2797G>T (p.Ala933Ser) | COSMIC COSMIC |
X | g.153954693C>G | CA415119790 | HCFC1 | c.3706G>C (p.Ala1236Pro) c.3508G>C (p.Ala1170Pro) c.2797G>C (p.Ala933Pro) | |
X | g.153954693C>T | CA415119792 | HCFC1 | c.3706G>A (p.Ala1236Thr) c.3508G>A (p.Ala1170Thr) c.2797G>A (p.Ala933Thr) | |
X | g.153954694A>C | CA415119793 | HCFC1 | c.3705T>G (p.His1235Gln) c.3507T>G (p.His1169Gln) c.2796T>G (p.His932Gln) | |
X | g.153954694A>G | CA519702485 | HCFC1 | c.3705T>C (p.His1235=) c.3507T>C (p.His1169=) c.2796T>C (p.His932=) | |
X | g.153954694A>T | CA415119794 | HCFC1 | c.3705T>A (p.His1235Gln) c.3507T>A (p.His1169Gln) c.2796T>A (p.His932Gln) | |
X | g.153954695T>A | CA415119795 | HCFC1 | c.3704A>T (p.His1235Leu) c.3506A>T (p.His1169Leu) c.2795A>T (p.His932Leu) | |
X | g.153954695T>C | CA415119797 | HCFC1 | c.3704A>G (p.His1235Arg) c.3506A>G (p.His1169Arg) c.2795A>G (p.His932Arg) | |
X | g.153954695T>G | CA415119799 | HCFC1 | c.3704A>C (p.His1235Pro) c.3506A>C (p.His1169Pro) c.2795A>C (p.His932Pro) | |
X | g.153954696G>A | CA415119803 | HCFC1 | c.3703C>T (p.His1235Tyr) c.3505C>T (p.His1169Tyr) c.2794C>T (p.His932Tyr) | gnomAD v4 |
X | g.153954696G>C | CA415119801 | HCFC1 | c.3703C>G (p.His1235Asp) c.3505C>G (p.His1169Asp) c.2794C>G (p.His932Asp) | |
X | g.153954696G>T | CA415119802 | HCFC1 | c.3703C>A (p.His1235Asn) c.3505C>A (p.His1169Asn) c.2794C>A (p.His932Asn) | |
X | g.153954697G>A | CA519702494 | HCFC1 | c.3702C>T (p.Ser1234=) c.3504C>T (p.Ser1168=) c.2793C>T (p.Ser931=) | gnomAD v4 |
X | g.153954697G>C | CA415119804 | HCFC1 | c.3702C>G (p.Ser1234Arg) c.3504C>G (p.Ser1168Arg) c.2793C>G (p.Ser931Arg) | gnomAD v4 |
X | g.153954697G>T | CA415119805 | HCFC1 | c.3702C>A (p.Ser1234Arg) c.3504C>A (p.Ser1168Arg) c.2793C>A (p.Ser931Arg) | gnomAD v4 |
X | g.153954698C>A | CA415119806 | HCFC1 | c.3701G>T (p.Ser1234Ile) c.3503G>T (p.Ser1168Ile) c.2792G>T (p.Ser931Ile) | |
X | g.153954698C>G | CA415119807 | HCFC1 | c.3701G>C (p.Ser1234Thr) c.3503G>C (p.Ser1168Thr) c.2792G>C (p.Ser931Thr) | |
X | g.153954698C>T | CA415119808 | HCFC1 | c.3701G>A (p.Ser1234Asn) c.3503G>A (p.Ser1168Asn) c.2792G>A (p.Ser931Asn) | gnomAD v4 |
X | g.153954699T>A | CA415119809 | HCFC1 | c.3700A>T (p.Ser1234Cys) c.3502A>T (p.Ser1168Cys) c.2791A>T (p.Ser931Cys) | |
X | g.153954699T>C | CA415119810 | HCFC1 | c.3700A>G (p.Ser1234Gly) c.3502A>G (p.Ser1168Gly) c.2791A>G (p.Ser931Gly) | |
X | g.153954699T>G | CA415119811 | HCFC1 | c.3700A>C (p.Ser1234Arg) c.3502A>C (p.Ser1168Arg) c.2791A>C (p.Ser931Arg) | |
X | g.153954700G>A | CA10557152 | HCFC1 | c.3699C>T (p.His1233=) c.3501C>T (p.His1167=) c.2790C>T (p.His930=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
X | g.153954700G>C | CA415119815 | HCFC1 | c.3699C>G (p.His1233Gln) c.3501C>G (p.His1167Gln) c.2790C>G (p.His930Gln) | |
X | g.153954700G= | CA2466540243 | HCFC1 | c.3699C= (p.His1233=) c.3501C= (p.His1167=) c.2790C= (p.His930=) | |
X | g.153954700G>T | CA415119816 | HCFC1 | c.3699C>A (p.His1233Gln) c.3501C>A (p.His1167Gln) c.2790C>A (p.His930Gln) | gnomAD v4 |
X | g.153954701T>A | CA415119821 | HCFC1 | c.3698A>T (p.His1233Leu) c.3500A>T (p.His1167Leu) c.2789A>T (p.His930Leu) | |
X | g.153954701T>C | CA415119819 | HCFC1 | c.3698A>G (p.His1233Arg) c.3500A>G (p.His1167Arg) c.2789A>G (p.His930Arg) | dbSNP gnomAD v3 gnomAD v4 |
X | g.153954701T>G | CA415119817 | HCFC1 | c.3698A>C (p.His1233Pro) c.3500A>C (p.His1167Pro) c.2789A>C (p.His930Pro) | |
X | g.153954701T= | CA2466540244 | HCFC1 | c.3698A= (p.His1233=) c.3500A= (p.His1167=) c.2789A= (p.His930=) | |
X | g.153954702G>A | CA337252819 | HCFC1 | c.3697C>T (p.His1233Tyr) c.3499C>T (p.His1167Tyr) c.2788C>T (p.His930Tyr) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.153954702G>C | CA415119823 | HCFC1 | c.3697C>G (p.His1233Asp) c.3499C>G (p.His1167Asp) c.2788C>G (p.His930Asp) | |
X | g.153954702G= | CA2466540245 | HCFC1 | c.3697C= (p.His1233=) c.3499C= (p.His1167=) c.2788C= (p.His930=) | |
X | g.153954702G>T | CA415119825 | HCFC1 | c.3697C>A (p.His1233Asn) c.3499C>A (p.His1167Asn) c.2788C>A (p.His930Asn) | |
X | g.153954703G>A | CA519702506 | HCFC1 | c.3696C>T (p.Arg1232=) c.3498C>T (p.Arg1166=) c.2787C>T (p.Arg929=) | |
X | g.153954703G>C | CA519702507 | HCFC1 | c.3696C>G (p.Arg1232=) c.3498C>G (p.Arg1166=) c.2787C>G (p.Arg929=) | |
X | g.153954703G>T | CA519702508 | HCFC1 | c.3696C>A (p.Arg1232=) c.3498C>A (p.Arg1166=) c.2787C>A (p.Arg929=) | |
X | g.153954704C>A | CA415119828 | HCFC1 | c.3695G>T (p.Arg1232Leu) c.3497G>T (p.Arg1166Leu) c.2786G>T (p.Arg929Leu) | |
X | g.153954704C= | CA2466540246 | HCFC1 | c.3695G= (p.Arg1232=) c.3497G= (p.Arg1166=) c.2786G= (p.Arg929=) | |
X | g.153954704C>G | CA415119829 | HCFC1 | c.3695G>C (p.Arg1232Pro) c.3497G>C (p.Arg1166Pro) c.2786G>C (p.Arg929Pro) | |
X | g.153954704C>T | CA10557153 | HCFC1 | c.3695G>A (p.Arg1232His) c.3497G>A (p.Arg1166His) c.2786G>A (p.Arg929His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
X | g.153954705G>A | CA10557154 | HCFC1 | c.3694C>T (p.Arg1232Cys) c.3496C>T (p.Arg1166Cys) c.2785C>T (p.Arg929Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
X | g.153954705G>C | CA415119832 | HCFC1 | c.3694C>G (p.Arg1232Gly) c.3496C>G (p.Arg1166Gly) c.2785C>G (p.Arg929Gly) | |
X | g.153954705G= | CA2466540247 | HCFC1 | c.3694C= (p.Arg1232=) c.3496C= (p.Arg1166=) c.2785C= (p.Arg929=) | |
X | g.153954705G>T | CA415119834 | HCFC1 | c.3694C>A (p.Arg1232Ser) c.3496C>A (p.Arg1166Ser) c.2785C>A (p.Arg929Ser) | gnomAD v4 |
X | g.153954706C>A | CA519702509 | HCFC1 | c.3693G>T (p.Gly1231=) c.3495G>T (p.Gly1165=) c.2784G>T (p.Gly928=) | |
X | g.153954706C>G | CA519702514 | HCFC1 | c.3693G>C (p.Gly1231=) c.3495G>C (p.Gly1165=) c.2784G>C (p.Gly928=) | |
X | g.153954706C>T | CA519702512 | HCFC1 | c.3693G>A (p.Gly1231=) c.3495G>A (p.Gly1165=) c.2784G>A (p.Gly928=) | |
X | g.153954707C>A | CA415119836 | HCFC1 | c.3692G>T (p.Gly1231Val) c.3494G>T (p.Gly1165Val) c.2783G>T (p.Gly928Val) | |
X | g.153954707C= | CA2466540248 | HCFC1 | c.3692G= (p.Gly1231=) c.3494G= (p.Gly1165=) c.2783G= (p.Gly928=) | |
X | g.153954707C>G | CA415119838 | HCFC1 | c.3692G>C (p.Gly1231Ala) c.3494G>C (p.Gly1165Ala) c.2783G>C (p.Gly928Ala) | |
X | g.153954707C>T | CA415119840 | HCFC1 | c.3692G>A (p.Gly1231Glu) c.3494G>A (p.Gly1165Glu) c.2783G>A (p.Gly928Glu) | dbSNP gnomAD v2 gnomAD v4 |
X | g.153954708C>A | CA415119842 | HCFC1 | c.3691G>T (p.Gly1231Trp) c.3493G>T (p.Gly1165Trp) c.2782G>T (p.Gly928Trp) | |
X | g.153954708C>G | CA415119844 | HCFC1 | c.3691G>C (p.Gly1231Arg) c.3493G>C (p.Gly1165Arg) c.2782G>C (p.Gly928Arg) | |
X | g.153954708C>T | CA415119843 | HCFC1 | c.3691G>A (p.Gly1231Arg) c.3493G>A (p.Gly1165Arg) c.2782G>A (p.Gly928Arg) | gnomAD v4 |
X | g.153954709C>A | CA519702519 | HCFC1 | c.3690G>T (p.Ala1230=) c.3492G>T (p.Ala1164=) c.2781G>T (p.Ala927=) | gnomAD v4 |
X | g.153954709C= | CA2466540249 | HCFC1 | c.3690G= (p.Ala1230=) c.3492G= (p.Ala1164=) c.2781G= (p.Ala927=) | |
X | g.153954709C>G | CA519702520 | HCFC1 | c.3690G>C (p.Ala1230=) c.3492G>C (p.Ala1164=) c.2781G>C (p.Ala927=) | |
X | g.153954709C>T | CA206502 | HCFC1 | c.3690G>A (p.Ala1230=) c.3492G>A (p.Ala1164=) c.2781G>A (p.Ala927=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.153954710G>A | CA10557155 | HCFC1 | c.3689C>T (p.Ala1230Val) c.3491C>T (p.Ala1164Val) c.2780C>T (p.Ala927Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.153954710G>C | CA415119847 | HCFC1 | c.3689C>G (p.Ala1230Gly) c.3491C>G (p.Ala1164Gly) c.2780C>G (p.Ala927Gly) | |
X | g.153954710G= | CA2466540250 | HCFC1 | c.3689C= (p.Ala1230=) c.3491C= (p.Ala1164=) c.2780C= (p.Ala927=) | |
X | g.153954710G>T | CA415119848 | HCFC1 | c.3689C>A (p.Ala1230Glu) c.3491C>A (p.Ala1164Glu) c.2780C>A (p.Ala927Glu) | gnomAD v4 |
X | g.153954711C>A | CA415119851 | HCFC1 | c.3688G>T (p.Ala1230Ser) c.3490G>T (p.Ala1164Ser) c.2779G>T (p.Ala927Ser) | |
X | g.153954711C= | CA2466540251 | HCFC1 | c.3688G= (p.Ala1230=) c.3490G= (p.Ala1164=) c.2779G= (p.Ala927=) | |
X | g.153954711C>G | CA415119852 | HCFC1 | c.3688G>C (p.Ala1230Pro) c.3490G>C (p.Ala1164Pro) c.2779G>C (p.Ala927Pro) | |
X | g.153954711C>T | CA10557156 | HCFC1 | c.3688G>A (p.Ala1230Thr) c.3490G>A (p.Ala1164Thr) c.2779G>A (p.Ala927Thr) | dbSNP ExAC gnomAD v2 |
X | g.153954712A>C | CA519702528 | HCFC1 | c.3687T>G (p.Pro1229=) c.3489T>G (p.Pro1163=) c.2778T>G (p.Pro926=) | |
X | g.153954712A>G | CA519702529 | HCFC1 | c.3687T>C (p.Pro1229=) c.3489T>C (p.Pro1163=) c.2778T>C (p.Pro926=) | gnomAD v4 |
X | g.153954712A>T | CA519702530 | HCFC1 | c.3687T>A (p.Pro1229=) c.3489T>A (p.Pro1163=) c.2778T>A (p.Pro926=) | |
X | g.153954713G>A | CA10557157 | HCFC1 | c.3686C>T (p.Pro1229Leu) c.3488C>T (p.Pro1163Leu) c.2777C>T (p.Pro926Leu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.153954713G>C | CA415119855 | HCFC1 | c.3686C>G (p.Pro1229Arg) c.3488C>G (p.Pro1163Arg) c.2777C>G (p.Pro926Arg) | |
X | g.153954713G= | CA2466540252 | HCFC1 | c.3686C= (p.Pro1229=) c.3488C= (p.Pro1163=) c.2777C= (p.Pro926=) | |
X | g.153954713G>T | CA415119857 | HCFC1 | c.3686C>A (p.Pro1229His) c.3488C>A (p.Pro1163His) c.2777C>A (p.Pro926His) | |
X | g.153954714G>A | CA415119859 | HCFC1 | c.3685C>T (p.Pro1229Ser) c.3487C>T (p.Pro1163Ser) c.2776C>T (p.Pro926Ser) | ClinVar dbSNP gnomAD v4 |
X | g.153954714G>C | CA415119861 | HCFC1 | c.3685C>G (p.Pro1229Ala) c.3487C>G (p.Pro1163Ala) c.2776C>G (p.Pro926Ala) | |
X | g.153954714G= | CA2466540253 | HCFC1 | c.3685C= (p.Pro1229=) c.3487C= (p.Pro1163=) c.2776C= (p.Pro926=) | |
X | g.153954714G>T | CA415119862 | HCFC1 | c.3685C>A (p.Pro1229Thr) c.3487C>A (p.Pro1163Thr) c.2776C>A (p.Pro926Thr) | |
X | g.153954715A>C | CA519702534 | HCFC1 | c.3684T>G (p.Leu1228=) c.3486T>G (p.Leu1162=) c.2775T>G (p.Leu925=) | |
X | g.153954715A>G | CA519702535 | HCFC1 | c.3684T>C (p.Leu1228=) c.3486T>C (p.Leu1162=) c.2775T>C (p.Leu925=) | |
X | g.153954715A>T | CA519702536 | HCFC1 | c.3684T>A (p.Leu1228=) c.3486T>A (p.Leu1162=) c.2775T>A (p.Leu925=) | |
X | g.153954716A>C | CA415119868 | HCFC1 | c.3683T>G (p.Leu1228Arg) c.3485T>G (p.Leu1162Arg) c.2774T>G (p.Leu925Arg) | |
X | g.153954716A>G | CA415119864 | HCFC1 | c.3683T>C (p.Leu1228Pro) c.3485T>C (p.Leu1162Pro) c.2774T>C (p.Leu925Pro) | |
X | g.153954716A>T | CA415119866 | HCFC1 | c.3683T>A (p.Leu1228His) c.3485T>A (p.Leu1162His) c.2774T>A (p.Leu925His) | |
X | g.153954717G>A | CA10557158 | HCFC1 | c.3682C>T (p.Leu1228Phe) c.3484C>T (p.Leu1162Phe) c.2773C>T (p.Leu925Phe) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.153954717G>C | CA415119870 | HCFC1 | c.3682C>G (p.Leu1228Val) c.3484C>G (p.Leu1162Val) c.2773C>G (p.Leu925Val) | |
X | g.153954717G= | CA2466540254 | HCFC1 | c.3682C= (p.Leu1228=) c.3484C= (p.Leu1162=) c.2773C= (p.Leu925=) | |
X | g.153954717G>T | CA415119872 | HCFC1 | c.3682C>A (p.Leu1228Ile) c.3484C>A (p.Leu1162Ile) c.2773C>A (p.Leu925Ile) | |
X | g.153954718G>A | CA519702542 | HCFC1 | c.3681C>T (p.Asp1227=) c.3483C>T (p.Asp1161=) c.2772C>T (p.Asp924=) | dbSNP gnomAD v2 |
X | g.153954718G>C | CA415119874 | HCFC1 | c.3681C>G (p.Asp1227Glu) c.3483C>G (p.Asp1161Glu) c.2772C>G (p.Asp924Glu) | ClinVar |
X | g.153954718G= | CA2466540255 | HCFC1 | c.3681C= (p.Asp1227=) c.3483C= (p.Asp1161=) c.2772C= (p.Asp924=) | |
X | g.153954718G>T | CA415119875 | HCFC1 | c.3681C>A (p.Asp1227Glu) c.3483C>A (p.Asp1161Glu) c.2772C>A (p.Asp924Glu) | gnomAD v4 |
X | g.153954719T>A | CA415119877 | HCFC1 | c.3680A>T (p.Asp1227Val) c.3482A>T (p.Asp1161Val) c.2771A>T (p.Asp924Val) | |
X | g.153954719T>C | CA415119879 | HCFC1 | c.3680A>G (p.Asp1227Gly) c.3482A>G (p.Asp1161Gly) c.2771A>G (p.Asp924Gly) | |
X | g.153954719T>G | CA415119880 | HCFC1 | c.3680A>C (p.Asp1227Ala) c.3482A>C (p.Asp1161Ala) c.2771A>C (p.Asp924Ala) | |
X | g.153954720C>A | CA415119882 | HCFC1 | c.3679G>T (p.Asp1227Tyr) c.3481G>T (p.Asp1161Tyr) c.2770G>T (p.Asp924Tyr) | |
X | g.153954720C>G | CA415119883 | HCFC1 | c.3679G>C (p.Asp1227His) c.3481G>C (p.Asp1161His) c.2770G>C (p.Asp924His) | |
X | g.153954720C>T | CA415119885 | HCFC1 | c.3679G>A (p.Asp1227Asn) c.3481G>A (p.Asp1161Asn) c.2770G>A (p.Asp924Asn) | |
X | g.153954721C>A | CA415119886 | HCFC1 | c.3678G>T (p.Lys1226Asn) c.3480G>T (p.Lys1160Asn) c.2769G>T (p.Lys923Asn) | |
X | g.153954721C>G | CA415119887 | HCFC1 | c.3678G>C (p.Lys1226Asn) c.3480G>C (p.Lys1160Asn) c.2769G>C (p.Lys923Asn) | |
X | g.153954721C>T | CA519702547 | HCFC1 | c.3678G>A (p.Lys1226=) c.3480G>A (p.Lys1160=) c.2769G>A (p.Lys923=) | |
X | g.153954722T>A | CA415119888 | HCFC1 | c.3677A>T (p.Lys1226Met) c.3479A>T (p.Lys1160Met) c.2768A>T (p.Lys923Met) | |
X | g.153954722T>C | CA415119889 | HCFC1 | c.3677A>G (p.Lys1226Arg) c.3479A>G (p.Lys1160Arg) c.2768A>G (p.Lys923Arg) | |
X | g.153954722T>G | CA415119890 | HCFC1 | c.3677A>C (p.Lys1226Thr) c.3479A>C (p.Lys1160Thr) c.2768A>C (p.Lys923Thr) | |
X | g.153954723T>A | CA415119892 | HCFC1 | c.3676A>T (p.Lys1226Ter) c.3478A>T (p.Lys1160Ter) c.2767A>T (p.Lys923Ter) | |
X | g.153954723T>C | CA415119894 | HCFC1 | c.3676A>G (p.Lys1226Glu) c.3478A>G (p.Lys1160Glu) c.2767A>G (p.Lys923Glu) | |
X | g.153954723T>G | CA415119895 | HCFC1 | c.3676A>C (p.Lys1226Gln) c.3478A>C (p.Lys1160Gln) c.2767A>C (p.Lys923Gln) | |
X | g.153954724A>C | CA415119897 | HCFC1 | c.3675T>G (p.Ile1225Met) c.3477T>G (p.Ile1159Met) c.2766T>G (p.Ile922Met) | |
X | g.153954724A>G | CA519702551 | HCFC1 | c.3675T>C (p.Ile1225=) c.3477T>C (p.Ile1159=) c.2766T>C (p.Ile922=) | |
X | g.153954724A>T | CA519702552 | HCFC1 | c.3675T>A (p.Ile1225=) c.3477T>A (p.Ile1159=) c.2766T>A (p.Ile922=) | |
X | g.153954725A= | CA2466540256 | HCFC1 | c.3674T= (p.Ile1225=) c.3476T= (p.Ile1159=) c.2765T= (p.Ile922=) | |
X | g.153954725A>C | CA415119899 | HCFC1 | c.3674T>G (p.Ile1225Ser) c.3476T>G (p.Ile1159Ser) c.2765T>G (p.Ile922Ser) | |
X | g.153954725A>G | CA415119901 | HCFC1 | c.3674T>C (p.Ile1225Thr) c.3476T>C (p.Ile1159Thr) c.2765T>C (p.Ile922Thr) | ClinVar dbSNP |
X | g.153954725A>T | CA415119903 | HCFC1 | c.3674T>A (p.Ile1225Asn) c.3476T>A (p.Ile1159Asn) c.2765T>A (p.Ile922Asn) |