SNP - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Result Filters

Display Settings:

Summary

Format

Summary

Send to:

Choose Destination

File
Clipboard
Collections

Select item 3844441.

rs384444 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 7:94428312 (GRCh38)
7:94057624 (GRCh37)
Canonical SPDI:: NC_000007.14:94428311:T:C
Gene:: COL1A2 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0./0 (HapMap)
HGVS:: NC_000007.14:g.94428312T>C, NC_000007.13:g.94057624T>C, NG_007405.1:g.38752T>C, NM_000089.4:c.3546T>C, NM_000089.3:c.3546T>C

Supplemental Content

Search details

Recent activity

Clear Turn Off Turn On

rs384444 (1)
SNP

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...