Variant #0000802997 (NC_000007.13:g.150753863C>T, NM_003040.3:c.-3050C>T (SLC4A2))

Chromosome 7
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.150753863C>T
DNA change (hg38) -
Published as CDK5(NM_004935.3):c.215G>A (p.S72N)
ISCN -
DB-ID ASIC3_000005
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC4A2 NM_003040.3 ?/. - c.-3050C>T r.(?) p.(=)
ASIC3 NM_004769.3 ?/. - c.*4124C>T r.(=) p.(=)
CDK5 NM_004935.3 ?/. - c.215G>A r.(?) p.(Ser72Asn)


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