Variant #0000304897 (NC_000011.9:g.57106074T>C, NM_003146.2:c.-2990A>G (SSRP1))

Chromosome 11
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.57106074T>C
DNA change (hg38) g.57338600T>C
Published as P2RX3(NM_002559.4):c.50T>C (p.V17A)
ISCN -
DB-ID P2RX3_000001
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
P2RX3 NM_002559.3 ?/. - c.50T>C r.(?) p.(Val17Ala)
SSRP1 NM_003146.2 ?/. - c.-2990A>G r.(?) p.(=)


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