29988609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54542300-G-A

29988609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54542300-G-T

http://identifiers.org/hco/7/GRCh38#29988764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54542433-C-A

29988764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54542433-C-T

29988869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54542538-A-G

29988874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54542543-C-T

http://identifiers.org/hco/7/GRCh38#29988990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54542687-C-A

29988990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54542687-C-T

29988996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54542693-C-T

29989040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54542733-G-A

29989040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54542733-G-T

http://identifiers.org/hco/7/GRCh38#29989090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54542790-C-A

29989090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54542790-C-T

29989218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54542877-G-A

http://identifiers.org/hco/7/GRCh38#29989220-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54542879-A-C

http://identifiers.org/hco/7/GRCh38#29989296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#54542928-C-A

http://identifiers.org/hco/7/GRCh38#29989319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54542951-C-A

29989319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54542951-C-T

29989320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54542952-T-C

29989340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54542972-G-A

29989340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54542972-G-T

29989423-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54543072-G-C

29989494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54543124-G-A

29989545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54543130-G-A

29989545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54543130-G-T

29989554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54543139-T-C

29989670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54543247-T-C

29989693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54543270-C-T

29989726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54543302-G-A

29989726-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54543302-G-C

29989761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54543325-T-C

29989763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54543327-G-T

http://identifiers.org/hco/7/GRCh38#29989787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#54543346-C-A

29989787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54543346-C-T

29989790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54543349-C-T

http://identifiers.org/hco/7/GRCh38#29989793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#54543352-C-A

29989793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54543352-C-T

29989849-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54543401-T-A

29989849-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54543401-T-G

29989884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54543429-G-A

29989884-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54543429-G-C

29989884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54543429-G-T

http://identifiers.org/hco/7/GRCh38#29990053-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#54543596-A-C

http://identifiers.org/hco/7/GRCh38#29990135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#54543675-C-A

29990135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54543675-C-T

http://identifiers.org/hco/7/GRCh38#29990194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#54543734-C-A

29990194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54543734-C-T

29990277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54543809-T-C

29990277-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54543809-T-G

29990418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54543912-T-C

29990418-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54543912-T-G

29990426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54543920-T-C

http://identifiers.org/hco/7/GRCh38#29990432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54543937-C-A

29990432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54543937-C-T

http://identifiers.org/hco/7/GRCh38#29990433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54543938-C-A

29990433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54543938-C-T

29990615-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54544059-C-G

29991082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54544636-C-T

29991378-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54544930-A-T

29992711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54545190-G-T

29992723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54545204-A-G

29992742-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54545223-T-G

29992822-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54545302-A-T

29992852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54545332-G-A

29992906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54545376-A-G

30001949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54546646-G-T

30001970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54546665-C-T

30002062-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54546736-T-A

30002304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54546972-G-A

http://identifiers.org/hco/7/GRCh38#30002713-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54547281-A-C

30002734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54547296-T-C

30002748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54547310-G-A

30002771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54548143-A-G

30002792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54548164-T-C

30002926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54548377-G-A

30002926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54548377-G-T

http://identifiers.org/hco/7/GRCh38#30002946-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54548399-A-C

30002946-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54548399-A-T

30003574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54549280-G-T

30003639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54549343-A-G

30003696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54549397-T-C

30004523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54550672-C-T

30004733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54550883-A-G

30004756-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54550909-T-A

30004786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54550939-A-G

30005013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54551490-A-G

30005105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54551582-T-C

30005105-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54551582-T-G

30005205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54551680-A-G

30005207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54551682-A-G

30005328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54551797-A-G

http://identifiers.org/hco/7/GRCh38#30005364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54551832-C-A

30005364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54551832-C-T

30005509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54551981-T-C

http://identifiers.org/hco/7/GRCh38#30005754-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54552223-A-C

30005754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54552223-A-G

30005754-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54552223-A-T

30005901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54552380-G-A

30010271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54553892-A-G

30010346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54553970-A-G

30010353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54553977-T-C

30012397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54554912-A-G

30012655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54555120-T-C

30012724-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54555177-A-T

30012841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54555295-A-G

http://identifiers.org/hco/7/GRCh38#30012872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#54555314-C-A

30012872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54555314-C-T

30013003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54555434-C-T

http://identifiers.org/hco/7/GRCh38#30013081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#54555508-C-A

30013557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54555688-T-C

30013617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54555747-A-G

30013755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54555888-A-G

30014116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54555982-G-A

30014116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54555982-G-T

http://identifiers.org/hco/7/GRCh38#30014186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#54555990-C-A

30014186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54555990-C-T

30014206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54556010-A-G

30014217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54556021-A-G

http://identifiers.org/hco/7/GRCh38#30014255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#54556055-C-A

30014255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54556055-C-T

30014256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54556056-T-C

30014258-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54556058-A-T

30014357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54556154-T-C

30014392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54556194-G-T

30014421-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54556223-A-T

30014433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54556235-A-G

30014481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54556285-G-A

30014481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54556285-G-T

30014486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54556290-A-G

30014500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54556299-G-T

30014537-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54556331-T-G

30014572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54556366-T-C

30014573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54556370-G-A

30014588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54556386-T-C

30014687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54556467-T-C

30014728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54556506-T-C

30014747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54556525-G-A

30014747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54556525-G-T

30014831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54556609-A-G

30014831-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54556609-A-T

30014904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54556682-A-G

30018182-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54560857-T-G

30018459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54561637-G-T

30018518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54561701-A-G

http://identifiers.org/hco/7/GRCh38#30018519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#54561702-C-A

30018568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54561740-C-T

30018671-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54561835-G-C

30018727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54561885-C-T

http://identifiers.org/hco/7/GRCh38#30018954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#54562740-C-A

30018972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54562765-G-A

30018999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54562791-A-G

30019188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54562982-T-C

30019230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54563019-T-C

30019333-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54563136-C-G

30019333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54563136-C-T

30019432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54563203-T-C

30019700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54563466-C-T

http://identifiers.org/hco/7/GRCh38#30019847-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#54563591-A-C

30020070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54563833-T-C

http://identifiers.org/hco/7/GRCh38#30020165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#54563933-C-A

30020165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54563933-C-T

http://identifiers.org/hco/7/GRCh38#30020189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#54563957-C-A

30020189-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54563957-C-G

30020238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54564006-A-G

30020238-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54564006-A-T

30020411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54564157-G-A

30020411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54564157-G-T

30020726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54564224-G-A

30020957-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54564384-A-T

30021075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54564494-T-C

30021137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54564555-A-G

30021465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54564851-G-A

30022080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54565233-C-T

30022312-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54565429-T-G

30022684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54566277-G-A

30022684-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54566277-G-C

30022780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54566373-G-A

30022910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54566620-G-A

30022910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54566620-G-T

http://identifiers.org/hco/7/GRCh38#30022947-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#54566657-A-C

30023027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54566730-T-C

http://identifiers.org/hco/7/GRCh38#30023069-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#54566772-A-C

30023412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54567762-T-C

30023467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54567816-A-G

30023544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54567884-T-C

http://identifiers.org/hco/7/GRCh38#30025078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#54568763-C-A

30025260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54568930-G-A

30025260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54568930-G-T

30025435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54569047-G-A

30025435-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54569047-G-C

30025435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54569047-G-T

30025498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54569091-G-C

http://identifiers.org/hco/7/GRCh38#30025624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#54569166-C-A

30025694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54569233-T-C

30025787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54569321-T-C

http://identifiers.org/hco/7/GRCh38#30026455-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#54569975-A-C

30026455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 54569975-A-G

30026502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 54570022-G-A

30026575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 54570071-G-T

30026582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 54570078-G-A

30026593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 54570084-A-G

30026595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 54570086-G-A

30026595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 54570086-G-T

30026727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 54570228-T-C

30026780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: non coding transcript exon variant
orthologous variants: 54570281-T-C

30026790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: non coding transcript exon variant
orthologous variants: 54570291-T-C

30026805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 54570305-G-A

30026805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 54570305-G-T

30027227-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: non coding transcript exon variant
orthologous variants: 54571150-T-G

30027311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 54571226-A-G

30027420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: non coding transcript exon variant
orthologous variants: 54571348-G-T

30027477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40990
most severe consequence: non coding transcript exon variant
orthologous variants: 54571386-A-G