Variant #0000653942 (NC_000001.10:g.236180442A>G, NID1(NM_002508.2):c.2254+6T>C)

Chromosome 1
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.236180442A>G
DNA change (hg38) g.236017142A>G
Published as NID1(NM_002508.2):c.2254+6T>C
ISCN -
DB-ID NID1_000035
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner VKGL-NL_Rotterdam
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NID1 NM_002508.2 ?/. - c.2254+6T>C r.(=) p.(=)