http://identifiers.org/hco/2/GRCh38#218450352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74474789-C-A

http://identifiers.org/hco/2/GRCh38#218450381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74474817-C-A

218450381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74474817-C-T

218450488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74474923-G-A

218450499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74474933-G-A

218450607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74475028-A-G

218450635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74475051-C-T

http://identifiers.org/hco/2/GRCh38#218450645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74475061-C-A

218450796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74475188-C-T

218450864-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74475243-T-A

218451035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74475392-G-T

http://identifiers.org/hco/2/GRCh38#218451523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74475652-C-A

218451704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74475745-A-G

218451709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74475750-G-A

218451985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74475991-G-A

218451985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74475991-G-T

218451992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74476002-T-C

218452029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74476039-T-C

218452154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74476154-T-C

218452159-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74476159-T-A

218452159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74476159-T-C

218452299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74476292-T-C

http://identifiers.org/hco/2/GRCh38#218452313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74476305-C-A

http://identifiers.org/hco/2/GRCh38#218452316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74476308-C-A

218452316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74476308-C-T

218452400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74476385-T-C

218452785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74476743-T-C

218452998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74476950-A-G

218452998-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74476950-A-T

218453048-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74476995-T-A

218453061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74477008-T-C

218453085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74477029-A-G

218453090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74477034-T-C

218453115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74477057-T-C

218453141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74477076-G-A

218453141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74477076-G-T

218453144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74477079-T-C

218453148-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74477083-T-A

218453189-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74477123-G-C

218453218-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74477152-G-C

218453218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74477152-G-T

218453388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74477175-T-C

218453420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74477199-T-C

http://identifiers.org/hco/2/GRCh38#218453432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74477211-C-A

218453432-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74477211-C-G

218453432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74477211-C-T

218453636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74477380-C-T

218453876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74477536-T-C

218453966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74477620-T-C

218454119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74477765-A-G

218454147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74477792-G-T

218454190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74477834-A-G

http://identifiers.org/hco/2/GRCh38#218454216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74477858-C-A

218454334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74477955-G-A

218454334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74477955-G-T

http://identifiers.org/hco/2/GRCh38#218454467-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74478113-A-C

218454482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74478128-T-C

http://identifiers.org/hco/2/GRCh38#218454499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74478144-C-A

http://identifiers.org/hco/2/GRCh38#218454535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74478178-C-A

218454563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74478206-G-A

218454563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74478206-G-T

218454566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74478209-G-A

218454566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74478209-G-T

218454569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74478212-A-G

218454673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74478296-A-G

218454845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74478468-C-T

http://identifiers.org/hco/2/GRCh38#218454858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74478481-C-A

218454858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74478481-C-T

218454894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74478516-T-C

218454895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 3 prime UTR variant
orthologous variants: 74478517-A-G

218455058-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74478671-T-A

218455084-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74478696-G-C

218455084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74478696-G-T

218455141-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74478763-T-A

218455141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74478763-T-C

218455141-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74478763-T-G

218455158-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74478780-A-T

218455179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74478803-C-T

218455360-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74478945-A-T

http://identifiers.org/hco/2/GRCh38#218455535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74479077-C-A

218455535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74479077-C-T

http://identifiers.org/hco/2/GRCh38#218455550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74479097-C-A

218455550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74479097-C-T

218455597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: missense variant
orthologous variants: 74479136-G-C

218455597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: synonymous variant
orthologous variants: 74479136-G-T

218455687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: synonymous variant
orthologous variants: 74479226-C-T

218455711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: synonymous variant
orthologous variants: 74479250-G-A

218455733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74479272-A-G

218455733-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74479272-A-T

218456707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74480240-C-T

http://identifiers.org/hco/2/GRCh38#218456998-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74480597-A-C

218456998-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74480597-A-T

218457081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74480680-T-C

218457081-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74480680-T-G

218457179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74480777-G-A

218457179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74480777-G-T

218457220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74480811-G-T

218457261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74480850-G-A

218457261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74480850-G-T

218459692-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74483503-G-C

218459692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74483503-G-T

218459735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74483537-G-T

218459766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74483568-G-A

218459964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74483782-C-T

http://identifiers.org/hco/2/GRCh38#218460091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74483933-C-A

http://identifiers.org/hco/2/GRCh38#218460258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74483962-C-A

http://identifiers.org/hco/2/GRCh38#218460259-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74483963-A-C

218460314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74484022-T-C

218463349-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: missense variant
orthologous variants: 74489697-T-A

218463449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74489769-G-A

218463449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74489769-G-T

218463452-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74489772-G-C

218463452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74489772-G-T

218463497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74489817-A-G

218463497-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74489817-A-T

218463498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74489818-T-C

218465891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74491728-T-C

218465901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74491738-A-G

218465901-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74491738-A-T

http://identifiers.org/hco/2/GRCh38#218465909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74491746-C-A

218466067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: synonymous variant
orthologous variants: 74491903-C-T

218466172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 74492008-A-G

218473393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74492736-G-A

218474551-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74492912-T-G

218474871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 74493228-G-A

http://identifiers.org/hco/2/GRCh38#218474923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74493280-C-A

218476720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74495120-T-C

218476720-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74495120-T-G

218476752-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74495162-T-A

218476752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74495162-T-C

218476761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74495171-G-A

218476953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 74495351-A-G

http://identifiers.org/hco/2/GRCh38#218476958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74495356-C-A

218476958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74495356-C-T

218476984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 74495382-G-A

218476984-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 74495382-G-C

218476984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 74495382-G-T

218476993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74495391-G-A

218476993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74495391-G-T

http://identifiers.org/hco/2/GRCh38#218477070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74495505-C-A

218477070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74495505-C-T

218477101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74495558-G-A

218477101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74495558-G-T

218477113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74495624-G-T

218477129-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74495763-T-A

218477129-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74495763-T-G

218477312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74496086-G-A

218477404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74496176-A-G

218477411-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74496183-T-A

218477553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74496316-G-A

218478042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74497291-T-C

218478081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74497377-G-A

218478090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74497385-G-A

218478432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74497855-T-C

218479081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74498651-G-A

218479244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74498728-G-T

218479476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74498907-T-C

218479536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74498964-G-T

218479627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74499051-G-A

218479627-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74499051-G-C

http://identifiers.org/hco/2/GRCh38#218479808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74499235-C-A

218479808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74499235-C-T

218480658-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74499476-T-A

218480818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74499617-C-T

218481061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74500076-T-C

218481080-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74500095-C-G

218481117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74500130-A-G

http://identifiers.org/hco/2/GRCh38#218481172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74500180-C-A

218481189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74500194-A-G

218481979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74500655-A-G

218481985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74500661-T-C

218481985-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74500661-T-G

218482077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74500732-T-C

218482150-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 74500805-T-G

218482186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 74500841-C-G

218482186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 74500841-C-T

218482498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74501342-T-C

218482734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74502171-G-A

http://identifiers.org/hco/2/GRCh38#218482827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74502262-C-A

218482852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74502285-G-A

218482868-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74502309-C-G

218482868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74502309-C-T

218484789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74504586-C-T

218484796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74504596-T-C

http://identifiers.org/hco/2/GRCh38#218484832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74504632-C-A

218485758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74506170-A-G

218486015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74506420-A-G

http://identifiers.org/hco/2/GRCh38#218486020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74506425-C-A

218486071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74506467-G-T

218487222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74506989-T-C

218487230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74506996-C-T

218487860-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74507308-C-G

218487860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74507308-C-T

http://identifiers.org/hco/2/GRCh38#218488457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74507578-C-A

218488457-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74507578-C-G

218488457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74507578-C-T

218495685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74509624-G-A

218495685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74509624-G-C

218495685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74509624-G-T

218495705-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74509644-T-G

218495846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 74509782-T-C

218497710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74510434-C-T

218498206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74510871-G-A

218498206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74510871-G-T

218498224-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74510891-G-C

http://identifiers.org/hco/2/GRCh38#218498274-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74510939-A-C

218498274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74510939-A-G

http://identifiers.org/hco/2/GRCh38#218498282-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74510947-A-C

218498329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74510979-T-C

http://identifiers.org/hco/2/GRCh38#218507980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74512671-C-A

218508068-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74512755-G-C

218508090-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74512777-T-A

218508288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74513017-T-C

218508305-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74513047-T-G

218508320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74513070-C-T

218508356-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74513182-G-C

218509683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74513846-A-G

218509787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74513969-A-G

218510037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74514200-T-C

218510337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74514529-T-C

218510347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74514554-C-T

218510556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74514930-G-A

218529949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 74517199-T-C

218534540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74518755-G-A

218534909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74518996-C-T

218535003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74519079-T-C

218546177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74525096-A-G

218546193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74525112-C-T

218546312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74525233-A-G

http://identifiers.org/hco/2/GRCh38#218546342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74525263-C-A

http://identifiers.org/hco/2/GRCh38#218546357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74525278-C-A

218546781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74525656-T-C

218546833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74525703-A-G

http://identifiers.org/hco/2/GRCh38#218546907-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74525766-A-C

218547107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74525971-T-C

218547107-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74525971-T-G

218549769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74529209-T-C

http://identifiers.org/hco/2/GRCh38#218549918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74529358-C-A

218549918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74529358-C-T

http://identifiers.org/hco/2/GRCh38#218549948-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74529371-A-C

218549948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74529371-A-G

218549977-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74529400-T-A

http://identifiers.org/hco/2/GRCh38#218550021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74529438-C-A

218550185-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74529583-G-C

http://identifiers.org/hco/2/GRCh38#218553419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74531678-C-A

218553419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74531678-C-T

218553537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74532048-G-A

218553537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74532048-G-T

218553577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: missense variant
orthologous variants: 74532088-C-T

http://identifiers.org/hco/2/GRCh38#218553753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74532302-C-A

218553792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74532336-A-G

218557953-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74534463-T-A

218557953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74534463-T-C

218557953-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74534463-T-G

218558163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74534619-G-A

218558178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74534634-G-A

218558552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 74534843-A-G

218558553-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, missense_variant
orthologous variants: 74534844-T-A

218558553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, missense_variant
orthologous variants: 74534844-T-C

218558585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 74534876-T-C

218558594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 74534885-T-C

http://identifiers.org/hco/2/GRCh38#218558600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74534891-C-A

218558612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 74534903-A-G

218558617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, stop_gained
orthologous variants: 74534908-G-A

218558617-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, missense_variant
orthologous variants: 74534908-G-C

218558636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, missense_variant
orthologous variants: 74534927-T-C

218558645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 74534936-A-G

218558655-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 74534946-T-A

218558655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 74534946-T-C

218558668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 74534963-T-C

218558682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 74534977-A-G

218558817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74535197-T-C

218559443-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74535446-C-G

218559505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74535510-C-T

218560046-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74535979-A-T

218560122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74536043-G-A

http://identifiers.org/hco/2/GRCh38#218560221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74536138-C-A

218560269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74536187-C-T

218560396-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74536299-C-G

http://identifiers.org/hco/2/GRCh38#218560448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74536404-C-A

218560448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74536404-C-T

218560826-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 5 prime UTR variant
orthologous variants: 74536738-G-C

218560999-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74536912-G-C

218560999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74536912-G-T

218561025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74536932-G-T

218561250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74537141-A-G

218561320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74537205-T-C

218561767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74537524-T-C

218561897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74537650-A-G

218562185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74538592-C-T

218562567-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74539003-T-A

218562567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74539003-T-C

218562568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74539004-G-A

218562568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74539004-G-T

http://identifiers.org/hco/2/GRCh38#218562578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74539020-C-A

218563336-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74539438-G-C

218563360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74539470-G-A

218563460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74539566-A-G

218564604-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74540613-T-A

218564604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74540613-T-C

218564653-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74540661-G-C

218564822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74540780-C-T

http://identifiers.org/hco/2/GRCh38#218565160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74541056-C-A

218565160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74541056-C-T

http://identifiers.org/hco/2/GRCh38#218565208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74541105-C-A

218565257-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74541143-C-G

218565267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74541153-T-C

218565362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74541245-A-G

218565363-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74541246-G-C

218565770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74542306-T-C

218565786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74542322-C-T

http://identifiers.org/hco/2/GRCh38#218565980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74542556-C-A

218565980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74542556-C-T

218566568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74543218-G-A

218566568-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74543218-G-C

218566657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74543303-T-C

http://identifiers.org/hco/2/GRCh38#218566887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74543704-C-A

218566887-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74543704-C-G

218567502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74544180-T-C

218567789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74544435-G-T

218567935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74544587-G-A

218567943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74544595-T-C

218567943-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74544595-T-G

218567980-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74544629-T-A

218568043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74544685-A-G

218568062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74544704-G-A

218568062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74544704-G-T

http://identifiers.org/hco/2/GRCh38#218568101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74544740-C-A

218568123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74544762-G-A

218568172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: intron variant
orthologous variants: 74544813-C-T

http://identifiers.org/hco/2/GRCh38#218568181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74544822-C-A

218568181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 5 prime UTR variant
orthologous variants: 74544822-C-T

218568259-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 5 prime UTR variant
orthologous variants: 74544899-G-C

218568259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 5 prime UTR variant
orthologous variants: 74544899-G-T

218568287-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 5 prime UTR variant
orthologous variants: 74544930-G-C

218568287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20063
most severe consequence: 5 prime UTR variant
orthologous variants: 74544930-G-T