Variant #0000621303 (NC_000003.11:g.52867732G>A, NM_002218.4:c.-3074C>T (ITIH4))

Chromosome 3
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.52867732G>A
DNA change (hg38) g.52833716G>A
Published as MUSTN1(NM_205853.4):c.43C>T (p.R15C), TMEM110-MUSTN1(NM_001198974.2):c.913C>T (p.R305C)
ISCN -
DB-ID ITIH4_000003
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00013 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2022-05-09 15:51:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TMEM110-MUSTN1 NM_001198974.1 ?/. - c.913C>T r.(?) p.(Arg305Cys)
ITIH4 NM_002218.4 ?/. - c.-3074C>T r.(?) p.(=)
TMEM110 NM_198563.2 ?/. - c.*6778C>T r.(=) p.(=)
MUSTN1 NM_205853.3 ?/. - c.43C>T r.(?) p.(Arg15Cys)


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