Variant #0000689696 (NC_000006.11:g.31913046C>T, NM_000063.4:c.2171C>T (C2))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.31913046C>T
DNA change (hg38) -
Published as C2(NM_000063.6):c.2171C>T (p.P724L), C2(NM_001282458.1):c.2084C>T (p.P695L)
ISCN -
DB-ID C2_000035 See all 2 reported entries
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) 0.00018 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C2 NM_000063.4 -?/. - c.2171C>T r.(?) p.(Pro724Leu)
CFB NM_001710.5 -?/. - c.-953C>T r.(?) p.(=)
ZBTB12 NM_181842.2 -?/. - c.-43453G>A r.(?) p.(=)


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