rs1061170

Associated Genes

Type

Snp

Classification

Missense

Locations

AssemblySequencePositionAllelesSource
GRCh38NC_000001.11(opens in new window)196690107
  • C > A
  • C > G
  • C > T
dbSnp
GRCh37NC_000001.10(opens in new window)196659237
  • C > A
  • C > G
  • C > T
dbSnp
NG_007259.1(opens in new window)43097
  • C > A
  • C > G
  • C > T
dbSnp
NP_000177.2(opens in new window)402
  • H > D
  • H > N
  • H > Y
dbSnp

Variant Frequencies

Identifiers

PharmGKB ID

PA166153617

Aliases

  • rs60173482 (retired)
  • NC_000001.10:g.196659237C=
  • NC_000001.10:g.196659237C>T
  • NC_000001.11:g.196690107C=
  • NC_000001.11:g.196690107C>T
  • NG_007259.1:g.43097C=
  • NG_007259.1:g.43097C>T
  • NM_000186.3:c.1204C=
  • NM_000186.3:c.1204C>T
  • NM_001014975.2:c.1204C=
  • NM_001014975.2:c.1204C>T
  • NP_000177.2:p.His402=
  • NP_000177.2:p.His402Tyr
  • NP_001014975.1:p.His402=
  • NP_001014975.1:p.His402Tyr
  • XM_005245111.1:c.1204C=
  • XM_005245111.1:c.1204C>T
  • XM_005245112.1:c.1204C=
  • XM_005245112.1:c.1204C>T
  • XP_005245168.1:p.His402=
  • XP_005245168.1:p.His402Tyr
  • XP_005245169.1:p.His402=
  • XP_005245169.1:p.His402Tyr
  • rs60173482

History

No history available.