34669010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: 5 prime UTR variant
orthologous variants: 92295047-A-G

34669297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: 5 prime UTR variant
orthologous variants: 92295292-A-G

34669297-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: 5 prime UTR variant
orthologous variants: 92295292-A-T

34669298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: 5 prime UTR variant
orthologous variants: 92295293-G-T

34669435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: missense variant
orthologous variants: 92295388-G-A

34669435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: missense variant
orthologous variants: 92295388-G-T

34669632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: missense variant
orthologous variants: 92295588-G-A

34669632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: stop gained
orthologous variants: 92295588-G-T

34669734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: missense variant
orthologous variants: 92295644-G-A

34669734-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: missense variant
orthologous variants: 92295644-G-C

34669734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: missense variant
orthologous variants: 92295644-G-T

34669737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: missense variant
orthologous variants: 92295647-G-A

34669737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: missense variant
orthologous variants: 92295647-G-T

http://identifiers.org/hco/21/GRCh38#34669789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92295667-C-A

34669789-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: missense variant
orthologous variants: 92295667-C-G

34669789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: missense variant
orthologous variants: 92295667-C-T

34669801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: missense variant
orthologous variants: 92295679-A-G

34669801-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: missense variant
orthologous variants: 92295679-A-T

34669944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: missense variant
orthologous variants: 92295725-G-A

34669944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: missense variant
orthologous variants: 92295725-G-T

http://identifiers.org/hco/21/GRCh38#34669963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92295733-C-A

34669963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: missense variant
orthologous variants: 92295733-C-T

34669990-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: missense variant
orthologous variants: 92295745-A-T

34670022-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: missense variant
orthologous variants: 92295769-G-C

34670117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: synonymous variant
orthologous variants: 92295846-G-A

34670248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: missense variant
orthologous variants: 92295919-G-T

34670325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: missense variant
orthologous variants: 92295996-G-A

34670325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: missense variant
orthologous variants: 92295996-G-T

34670341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: missense variant
orthologous variants: 92296012-G-A

34670341-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: missense variant
orthologous variants: 92296012-G-C

34670341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: missense variant
orthologous variants: 92296012-G-T

34670358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: missense variant
orthologous variants: 92296029-G-A

34670358-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: missense variant
orthologous variants: 92296029-G-C

34670358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: missense variant
orthologous variants: 92296029-G-T

http://identifiers.org/hco/21/GRCh38#34670369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92296046-C-A

34670369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: synonymous variant
orthologous variants: 92296046-C-T

34670382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: missense variant
orthologous variants: 92296065-G-A

34670382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: stop gained
orthologous variants: 92296065-G-T

http://identifiers.org/hco/21/GRCh38#34670413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92296096-C-A

34670413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: missense variant
orthologous variants: 92296096-C-T

34670473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: missense variant
orthologous variants: 92296156-G-A

34670473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: missense variant
orthologous variants: 92296156-G-T

34670515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: missense variant
orthologous variants: 92296198-G-A

34670515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: missense variant
orthologous variants: 92296198-G-T

34670541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: missense variant
orthologous variants: 92296224-G-A

34670541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: stop gained
orthologous variants: 92296224-G-T

34670561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: missense variant
orthologous variants: 92296235-G-T

34670646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: missense_variant, undefined
orthologous variants: 92296329-G-A

34670646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: stop_gained, undefined
orthologous variants: 92296329-G-T

34670661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: missense_variant, undefined
orthologous variants: 92296344-G-A

34670661-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: missense_variant, undefined
orthologous variants: 92296344-G-C

34670661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: missense_variant, undefined
orthologous variants: 92296344-G-T

http://identifiers.org/hco/21/GRCh38#34670690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#92296373-C-A

34670690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: synonymous_variant, undefined
orthologous variants: 92296373-C-T

http://identifiers.org/hco/21/GRCh38#34670727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92296410-C-A

34670727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: synonymous variant
orthologous variants: 92296410-C-T

34670729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: synonymous variant
orthologous variants: 92296412-G-A

34670729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: synonymous variant
orthologous variants: 92296412-G-T

34670744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: synonymous variant
orthologous variants: 92296427-C-T

http://identifiers.org/hco/21/GRCh38#34670799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92296487-C-A

34670799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92296487-C-T

34670870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92296573-A-G

34670872-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92296575-T-A

34670872-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92296575-T-G

34670876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92296579-A-G

http://identifiers.org/hco/21/GRCh38#34670882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#92296585-C-A

34670882-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron_variant, undefined
orthologous variants: 92296585-C-G

34670882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron_variant, undefined
orthologous variants: 92296585-C-T

34670886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron_variant, undefined
orthologous variants: 92296586-T-C

34670890-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron_variant, undefined
orthologous variants: 92296590-T-A

34670890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron_variant, undefined
orthologous variants: 92296590-T-C

34670891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron_variant, undefined
orthologous variants: 92296591-G-T

34670916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92296596-G-A

34670916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92296596-G-T

34671050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92296684-A-G

34671088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92296722-G-A

34671126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92296738-A-G

34671126-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92296738-A-T

34671742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92297344-C-T

34671880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92297457-T-C

34672235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92297732-T-C

34672451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92297954-T-C

34672765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92298171-G-A

34672806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92298179-T-C

34672853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92298217-G-T

34672892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92298255-T-C

34673131-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron_variant, undefined
orthologous variants: 92298482-T-A

34673188-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron_variant, undefined
orthologous variants: 92298522-C-G

34674524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92299266-C-T

http://identifiers.org/hco/21/GRCh38#34674762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92299558-C-A

34674964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92299731-A-G

34675593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92300388-G-A

34675593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92300388-G-T

34675594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92300389-G-A

34675779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92300580-A-G

34675791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92300611-G-T

34675824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92300630-A-G

34675970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92300809-A-G

34675983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92300824-A-G

34676498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92301781-C-T

http://identifiers.org/hco/21/GRCh38#34676600-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92301875-A-C

34676603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92301878-G-A

34676739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92301997-C-T

34678709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92303000-G-A

34678734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92303025-A-G

34678746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92303037-T-C

34678807-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92303095-T-A

34678807-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92303095-T-G

34678838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92303117-T-C

http://identifiers.org/hco/21/GRCh38#34678971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92303259-C-A

34678972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92303260-T-C

http://identifiers.org/hco/21/GRCh38#34679046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92303329-C-A

http://identifiers.org/hco/21/GRCh38#34685687-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92305385-A-C

34685849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92305520-T-C

34685865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92305536-G-T

34685893-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92305565-T-G

34687013-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92307626-C-G

34687066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92307679-A-G

34687247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92307854-A-G

34687503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92308107-T-C

34687768-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92308357-T-A

34687982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92308523-C-T

34688183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92308703-T-C

34688262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92308763-G-A

http://identifiers.org/hco/21/GRCh38#34688392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92308839-C-A

34688392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92308839-C-T

34688606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92309040-A-G

34688739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92309157-G-A

34688906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92309300-G-A

http://identifiers.org/hco/21/GRCh38#34689022-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92311672-A-C

34689213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92311995-G-A

http://identifiers.org/hco/21/GRCh38#34689262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92312043-C-A

34689766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92312176-C-T

http://identifiers.org/hco/21/GRCh38#34689879-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92312290-A-C

34689892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92312303-G-A

34689915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92312326-C-T

34689921-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92312332-C-G

34689921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92312332-C-T

34690033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92312368-A-G

34690082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92312410-C-T

34690087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92312415-G-A

34690087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92312415-G-T

34690110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92312438-A-G

34690152-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92312481-G-C

34690161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92312495-G-A

34690204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92312537-G-A

34690230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92312555-G-T

34690292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92312612-G-A

http://identifiers.org/hco/21/GRCh38#34690584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#92312878-C-A

34690584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron_variant, undefined
orthologous variants: 92312878-C-T

34690606-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92312899-A-T

34690668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92312951-T-C

http://identifiers.org/hco/21/GRCh38#34690730-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92313013-A-C

34690736-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92313019-T-A

34690866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92313146-A-G

34691040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92313298-C-T

34691569-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92313786-T-A

34691569-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92313786-T-G

34691635-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92313838-T-G

http://identifiers.org/hco/21/GRCh38#34691749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92313949-C-A

34691752-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92313952-A-T

34691920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92314948-T-C

34692113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92315330-G-A

34692147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92315365-T-C

34692183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92315399-G-A

34692203-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92315419-T-G

34692217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92315433-A-G

34692497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92315696-G-A

34692740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92315936-G-A

34692871-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92316021-G-C

34692946-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92316072-T-G

34692960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92316086-C-T

34692977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92316104-C-T

34693074-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92316186-G-C

34693082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92316194-C-T

34693094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92316206-A-G

http://identifiers.org/hco/21/GRCh38#34693318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92316805-C-A

http://identifiers.org/hco/21/GRCh38#34693349-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92316831-A-C

34693397-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron_variant, undefined
orthologous variants: 92316876-G-C

34694812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92317115-G-A

34695054-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92317344-C-G

34695055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92317345-C-T

34695097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92317385-G-A

34695202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92317455-G-T

34695230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92317483-C-T

34695231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92317484-G-A

http://identifiers.org/hco/21/GRCh38#34695278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92317525-C-A

34695306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92317553-G-A

34695522-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92317757-C-G

34695522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92317757-C-T

http://identifiers.org/hco/21/GRCh38#34695571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#92317802-C-A

34695571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron_variant, undefined
orthologous variants: 92317802-C-T

34695937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron_variant, undefined
orthologous variants: 92318004-G-A

34696013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92318107-T-C

34696055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92318170-G-A

34696062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92318177-G-A

34696110-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92318252-C-G

34696111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92318253-C-T

34696521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92319113-C-T

34696657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92319265-T-C

http://identifiers.org/hco/21/GRCh38#34696755-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92319371-A-C

34696772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92319391-A-G

http://identifiers.org/hco/21/GRCh38#34696836-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92319454-A-C

34696836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92319454-A-G

34696845-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92319463-A-T

34696942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92319551-C-T

34697107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92319707-G-A

34697138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92319738-G-A

34697278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92319879-C-T

34697283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92319884-G-A

34697283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92319884-G-T

34697317-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92319912-G-C

34697569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92320124-G-A

34697648-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92320198-G-C

34697655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92320205-C-T

34701445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92320659-G-A

34701754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92321492-G-A

34701935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92321663-T-C

34701963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92321693-G-A

34701967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92321697-G-A

34702004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92321734-A-G

34702005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92321735-A-G

34702058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92321787-T-C

http://identifiers.org/hco/21/GRCh38#34702091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92321816-C-A

http://identifiers.org/hco/21/GRCh38#34702122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92321848-C-A

34702314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron_variant, undefined
orthologous variants: 92322039-A-G

34703643-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92322343-C-G

34703646-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92322346-G-C

34703867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92322560-T-C

34704072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92322789-G-A

34704120-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92322824-G-C

34704434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron_variant, undefined
orthologous variants: 92323135-C-T

34704557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92323251-G-A

http://identifiers.org/hco/21/GRCh38#34704640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92323340-C-A

34704674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92323372-A-G

34704849-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92323894-C-G

http://identifiers.org/hco/21/GRCh38#34704863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92323908-C-A

34704863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92323908-C-T

http://identifiers.org/hco/21/GRCh38#34705056-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92324104-A-C

34705204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92324260-G-A

34705218-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92324276-T-G

34705242-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92324302-T-G

34705276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92324329-C-T

34705333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92324379-A-G

http://identifiers.org/hco/21/GRCh38#34707179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92324815-C-A

34707179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92324815-C-T

34707185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92324821-T-C

34707217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92324853-T-C

34707217-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92324853-T-G

34707255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92324892-T-C

34707255-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92324892-T-G

http://identifiers.org/hco/21/GRCh38#34707262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92324899-C-A

34707262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92324899-C-T

34707275-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 92324943-T-G

34707291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: synonymous variant
orthologous variants: 92324959-T-C

34707294-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: synonymous variant
orthologous variants: 92324962-T-A

34707294-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: synonymous variant
orthologous variants: 92324962-T-G

http://identifiers.org/hco/21/GRCh38#34707396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92325064-C-A

34707396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 92325064-C-T

34707405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92325073-T-C

34707411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92325079-A-G

34707436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92325104-T-C

http://identifiers.org/hco/21/GRCh38#34707842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92325483-C-A

34707866-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron_variant, undefined
orthologous variants: 92325506-T-G

34708089-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron_variant, undefined
orthologous variants: 92325729-T-A

34708435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron_variant, undefined
orthologous variants: 92326513-G-A

34708536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92326592-T-C

34708576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92326630-A-G

34708576-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92326630-A-T

34708582-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92326636-A-T

34708605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92326659-T-C

34708605-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92326659-T-G

34708643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92326701-T-C

34708650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92326708-T-C

http://identifiers.org/hco/21/GRCh38#34708660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92326717-C-A

34708739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: synonymous variant
orthologous variants: 92326796-C-T

34708836-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92326888-T-A

34708836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92326888-T-C

http://identifiers.org/hco/21/GRCh38#34708867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92326915-C-A

34708867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92326915-C-T

34708883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92326944-T-C

http://identifiers.org/hco/21/GRCh38#34708888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92326949-C-A

http://identifiers.org/hco/21/GRCh38#34708941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92327004-C-A

34708941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92327004-C-T

http://identifiers.org/hco/21/GRCh38#34708945-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92327008-A-C

34709058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92327119-A-G

34709109-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92327169-T-A

http://identifiers.org/hco/21/GRCh38#34709262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92327527-C-A

34709262-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92327527-C-G

http://identifiers.org/hco/21/GRCh38#34709286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92327570-C-A

http://identifiers.org/hco/21/GRCh38#34709323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92327610-C-A

34709323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92327610-C-T

34709484-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: synonymous variant
orthologous variants: 92327771-G-C

34709484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: synonymous variant
orthologous variants: 92327771-G-T

34709502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: synonymous variant
orthologous variants: 92327789-T-C

34709502-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: synonymous variant
orthologous variants: 92327789-T-G

34709564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92327850-G-A

34709609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92327908-G-T

34709627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92327926-A-G

34710348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92328525-C-T

34710414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92328591-G-A

34710414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92328591-G-T

34710420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92328597-A-G

34711650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92329095-C-T

http://identifiers.org/hco/21/GRCh38#34711699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92329135-C-A

34711699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92329135-C-T

34711786-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92329206-G-C

34712093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92330054-G-A

34712215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92330186-T-C

34712935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron_variant, undefined
orthologous variants: 92330914-G-A

34712939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron_variant, undefined
orthologous variants: 92330918-C-T

34713396-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92331370-G-C

34713411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92331384-A-G

34713431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92331404-C-T

34715153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92334867-G-A

34715171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92334885-A-G

34715293-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92335004-A-T

34715650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92335341-A-G

34715756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92335446-G-A

34715891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92335564-G-T

34716182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92336196-T-C

http://identifiers.org/hco/21/GRCh38#34716191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92336205-C-A

34716191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92336205-C-T

http://identifiers.org/hco/21/GRCh38#34716218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92336232-C-A

34716218-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92336232-C-G

34716264-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92336268-T-A

34716294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92336298-T-C

http://identifiers.org/hco/21/GRCh38#34716301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92336303-C-A

34716301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: intron variant
orthologous variants: 92336303-C-T

34716334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: missense variant
orthologous variants: 92336336-A-G

http://identifiers.org/hco/21/GRCh38#34716350-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92336352-A-C

34716350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: synonymous variant
orthologous variants: 92336352-A-G

34716368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: synonymous variant
orthologous variants: 92336370-T-C

34716461-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: missense variant
orthologous variants: 92336463-T-A

34716461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: synonymous variant
orthologous variants: 92336463-T-C

34716461-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: missense variant
orthologous variants: 92336463-T-G

34716484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: 3 prime UTR variant
orthologous variants: 92336486-G-A

34716620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: 3 prime UTR variant
orthologous variants: 92336787-A-G

34716628-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: 3 prime UTR variant
orthologous variants: 92336795-T-A

34716666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: 3 prime UTR variant
orthologous variants: 92336823-A-G

34716807-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: 3 prime UTR variant
orthologous variants: 92336940-A-T

34716817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: 3 prime UTR variant
orthologous variants: 92336950-T-C

34716817-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: 3 prime UTR variant
orthologous variants: 92336950-T-G

34716977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: 3 prime UTR variant
orthologous variants: 92337072-T-C

34717073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: 3 prime UTR variant
orthologous variants: 92337133-G-A

34717202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: 3 prime UTR variant
orthologous variants: 92337246-G-A

34717202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: 3 prime UTR variant
orthologous variants: 92337246-G-T

34717262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: 3 prime UTR variant
orthologous variants: 92337312-A-G

34717312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: 3 prime UTR variant
orthologous variants: 92337367-A-G

34717496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: 3 prime UTR variant
orthologous variants: 92337538-G-A

http://identifiers.org/hco/21/GRCh38#34717573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92337598-C-A

34717573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: 3 prime UTR variant
orthologous variants: 92337598-C-T

http://identifiers.org/hco/21/GRCh38#34717583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92337608-C-A

34717583-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: 3 prime UTR variant
orthologous variants: 92337608-C-G

34717730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: 3 prime UTR variant
orthologous variants: 92337704-A-G

http://identifiers.org/hco/21/GRCh38#34717739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92337711-C-A

34717782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: 3 prime UTR variant
orthologous variants: 92337750-G-T

34717997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: 3 prime UTR variant
orthologous variants: 92337931-T-C

34717997-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: 3 prime UTR variant
orthologous variants: 92337931-T-G

34718180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2065
most severe consequence: 3 prime UTR variant
orthologous variants: 92338101-T-C