http://identifiers.org/hco/16/GRCh38#2275933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24629119-C-A

2275933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: 3 prime UTR variant
orthologous variants: 24629119-C-T

2276028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: 3 prime UTR variant
orthologous variants: 24629019-G-A

2276028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: 3 prime UTR variant
orthologous variants: 24629019-G-T

http://identifiers.org/hco/16/GRCh38#2276079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24628976-C-A

2276079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: 3 prime UTR variant
orthologous variants: 24628976-C-T

http://identifiers.org/hco/16/GRCh38#2276135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24628903-C-A

http://identifiers.org/hco/16/GRCh38#2276147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24628890-C-A

http://identifiers.org/hco/16/GRCh38#2276156-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24628881-A-C

2276156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: 3 prime UTR variant
orthologous variants: 24628881-A-G

2276238-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: 3 prime UTR variant
orthologous variants: 24628793-C-G

2276239-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: 3 prime UTR variant
orthologous variants: 24628792-T-A

2276239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: 3 prime UTR variant
orthologous variants: 24628792-T-C

2276268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: 3 prime UTR variant
orthologous variants: 24628764-G-A

2276268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: 3 prime UTR variant
orthologous variants: 24628764-G-T

2276355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: 3 prime UTR variant
orthologous variants: 24628676-C-T

2276407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: 3 prime UTR variant
orthologous variants: 24628644-G-A

2276407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: 3 prime UTR variant
orthologous variants: 24628644-G-T

2276611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: 3 prime UTR variant
orthologous variants: 24628434-G-A

2276611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: 3 prime UTR variant
orthologous variants: 24628434-G-T

2276955-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: 24628111-T-A

2276955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: 24628111-T-C

2277404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: 24628059-C-T

2277432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: 24628032-G-C

http://identifiers.org/hco/16/GRCh38#2277446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24628018-C-A

2277446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: 24628018-C-T

2277469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: 24627995-G-T

2277474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: 24627990-A-G

2277474-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: 24627990-A-T

http://identifiers.org/hco/16/GRCh38#2277496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24627970-C-A

2277496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: 24627970-C-T

http://identifiers.org/hco/16/GRCh38#2277515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24627952-C-A

2277515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: 24627952-C-T

2277544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: 24627924-G-A

2277681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: 24627786-G-A

2277707-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: 24627770-G-C

2277853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: 24627712-T-C

2277868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: 24627710-C-T

2277905-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense variant
orthologous variants: 24627673-T-A

2277905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense variant
orthologous variants: 24627673-T-C

2277905-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense variant
orthologous variants: 24627673-T-G

2277920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense variant
orthologous variants: 24627658-G-A

2277920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense variant
orthologous variants: 24627658-G-T

http://identifiers.org/hco/16/GRCh38#2278164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24627392-C-A

2278164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: 24627392-C-T

http://identifiers.org/hco/16/GRCh38#2278165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24627391-C-A

2278165-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: 24627391-C-G

2278165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: 24627391-C-T

2278177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: 24627379-T-C

2278183-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: 24627374-A-T

http://identifiers.org/hco/16/GRCh38#2278375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24627164-C-A

2278375-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24627164-C-G

2278375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24627164-C-T

2278399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 24627140-A-G

http://identifiers.org/hco/16/GRCh38#2278546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#24627011-C-A

2278546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24627011-C-T

2278568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24626989-G-A

2278568-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24626989-G-C

2278568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24626989-G-T

2278600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24626957-G-A

2278600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24626957-G-T

2278773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24626854-G-A

http://identifiers.org/hco/16/GRCh38#2278802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24626835-C-A

2278802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24626835-C-T

2278878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24626792-C-T

2278937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24626734-G-A

2278937-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24626734-G-C

http://identifiers.org/hco/16/GRCh38#2279126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24626534-C-A

2279126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24626534-C-T

2279147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24626514-G-T

2279171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24626491-G-T

2279222-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24626450-C-G

2279222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24626450-C-T

2279226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24626446-G-T

http://identifiers.org/hco/16/GRCh38#2279243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24626429-C-A

2279243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24626429-C-T

2280521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24624828-C-T

2280668-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24624699-G-C

2280828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24624563-C-T

2280983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24624454-C-T

2281001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24624436-T-C

2281322-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24624168-C-G

2281362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24624130-C-T

2281499-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24624007-T-A

2281588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24623929-G-A

2281588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24623929-G-C

2281588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24623929-G-T

2281686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24623864-G-T

http://identifiers.org/hco/16/GRCh38#2282214-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24622566-A-C

2282240-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24622541-G-C

2282292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24622467-T-C

2282297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24622462-C-T

2282381-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24622380-G-C

2282576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24622164-C-T

2282986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24621643-C-T

http://identifiers.org/hco/16/GRCh38#2283017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24621611-C-A

2283017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24621611-C-T

2283065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24621524-G-A

2283065-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24621524-G-C

2283065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24621524-G-T

http://identifiers.org/hco/16/GRCh38#2283193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24621402-C-A

2283193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24621402-C-T

2283235-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24621360-A-T

2283361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 24621234-G-A

2283362-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 24621233-T-G

2283385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24621207-C-T

2283390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24621202-G-A

2284266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: 24619940-C-T

2284323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense variant
orthologous variants: 24619880-T-C

2284323-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense variant
orthologous variants: 24619880-T-G

2284326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense variant
orthologous variants: 24619877-C-T

http://identifiers.org/hco/16/GRCh38#2284459-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24619746-A-C

2284459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: 24619746-A-G

2284521-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: 24619701-G-C

2284760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: 24619618-G-A

2285031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: 24619344-G-A

2285109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: 24619321-G-T

2285125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: 24619307-C-T

2285129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: 24619303-A-G

2285237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: 24619229-G-T

2285300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: 24619195-A-G

2285373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: 24619126-G-A

http://identifiers.org/hco/16/GRCh38#2285390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24619110-C-A

2285390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: 24619110-C-T

2285392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: 24619108-A-G

2285403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: 24619098-G-A

2285403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: 24619098-G-T

2285408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: 24619093-C-T

http://identifiers.org/hco/16/GRCh38#2285455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24619048-C-A

2285496-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: synonymous variant
orthologous variants: 24619007-G-C

2285496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: synonymous variant
orthologous variants: 24619007-G-T

http://identifiers.org/hco/16/GRCh38#2285566-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24618937-A-C

2286623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: 24617638-C-T

2286713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense variant
orthologous variants: 24617561-C-T

2286715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense variant
orthologous variants: 24617559-G-A

2286715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense variant
orthologous variants: 24617559-G-T

http://identifiers.org/hco/16/GRCh38#2286730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24617544-C-A

2286730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense variant
orthologous variants: 24617544-C-T

2286764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense variant
orthologous variants: 24617510-C-T

2286765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: synonymous variant
orthologous variants: 24617509-G-A

2286968-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: splice acceptor variant
orthologous variants: 24617306-C-G

2287008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: 24617268-G-A

http://identifiers.org/hco/16/GRCh38#2287020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24617259-C-A

2287020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: 24617259-C-T

http://identifiers.org/hco/16/GRCh38#2287056-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24617224-A-C

2287056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: 24617224-A-G

2287066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: 24617170-G-A

2287066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: 24617170-G-C

2287066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: 24617170-G-T

2287070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: 24617166-G-A

2287070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: 24617166-G-T

2287974-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: 24616604-G-C

2287974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: 24616604-G-T

2287999-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: 24616586-C-G

http://identifiers.org/hco/16/GRCh38#2288003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24616582-C-A

http://identifiers.org/hco/16/GRCh38#2288004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24616581-C-A

http://identifiers.org/hco/16/GRCh38#2288008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24616577-C-A

2288008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron variant
orthologous variants: 24616577-C-T

2288061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense variant
orthologous variants: 24616526-A-G

http://identifiers.org/hco/16/GRCh38#2288281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24616306-C-A

2288281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense variant
orthologous variants: 24616306-C-T

2289349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24615690-G-T

http://identifiers.org/hco/16/GRCh38#2289388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24615659-C-A

2289388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24615659-C-T

2289394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24615653-G-A

2289394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24615653-G-T

http://identifiers.org/hco/16/GRCh38#2289414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24615634-C-A

http://identifiers.org/hco/16/GRCh38#2289459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24615583-C-A

2289459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24615583-C-T

2289512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 24615530-G-A

2289512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 24615530-G-T

2289641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24615403-A-G

http://identifiers.org/hco/16/GRCh38#2289659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24615385-C-A

2289659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24615385-C-T

2290315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24612881-G-A

2292113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24611985-G-A

2292113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24611985-G-T

2292115-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24611983-T-A

http://identifiers.org/hco/16/GRCh38#2292308-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24611793-A-C

2292308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24611793-A-G

http://identifiers.org/hco/16/GRCh38#2292312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24611720-C-A

2292312-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24611720-C-G

2292312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24611720-C-T

http://identifiers.org/hco/16/GRCh38#2292314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24611718-C-A

2292314-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24611718-C-G

2292314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24611718-C-T

http://identifiers.org/hco/16/GRCh38#2292315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24611717-C-A

2292315-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24611717-C-G

2292315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24611717-C-T

2292319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24611713-G-A

2292319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24611713-G-T

http://identifiers.org/hco/16/GRCh38#2292332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24611700-C-A

2292332-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24611700-C-G

2292332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24611700-C-T

http://identifiers.org/hco/16/GRCh38#2292333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24611699-C-A

2292372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24611661-G-T

2292373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24611660-G-A

2292373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24611660-G-T

http://identifiers.org/hco/16/GRCh38#2295451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24606668-C-A

2295451-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24606668-C-G

2295451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24606668-C-T

2295593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24606555-T-C

2295596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24606552-G-A

2295596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24606552-G-T

2295629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24606519-G-A

http://identifiers.org/hco/16/GRCh38#2295825-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24606349-A-C

http://identifiers.org/hco/16/GRCh38#2295889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24606290-C-A

2295889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24606290-C-T

2295942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24606238-G-A

2296064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24606137-G-A

2296159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24606066-C-T

2296565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24605972-G-A

2296686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24605870-A-G

2297302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24605405-C-T

2297490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24605203-C-T

http://identifiers.org/hco/16/GRCh38#2297511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24605182-C-A

2297576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24605112-G-T

2297577-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24605111-C-G

2297577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24605111-C-T

2297617-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24605072-C-G

2297617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24605072-C-T

2297657-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24605035-T-A

2297657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24605035-T-C

2297737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24604960-A-G

http://identifiers.org/hco/16/GRCh38#2297773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24604937-C-A

2297773-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24604937-C-G

2297773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24604937-C-T

2297836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24604874-C-T

2297950-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24604767-C-G

2297950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24604767-C-T

2298359-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24604554-C-G

2298452-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 24604458-C-G

2298452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 24604458-C-T

2298628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24604279-C-T

http://identifiers.org/hco/16/GRCh38#2298665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24604250-C-A

2298665-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24604250-C-G

2298665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24604250-C-T

2298678-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24604232-T-A

2298678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24604232-T-C

2298678-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24604232-T-G

2298761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24604144-C-T

2299251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24603671-G-A

2299251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24603671-G-T

http://identifiers.org/hco/16/GRCh38#2299305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24603639-C-A

2299305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24603639-C-T

2299317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24603617-A-G

2299317-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24603617-A-T

2299324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24603610-G-A

2299324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24603610-G-T

2299357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24603592-A-G

2299438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24603513-C-T

2299572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24603388-C-T

2299586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24603378-C-T

2299851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24603104-G-A

2299915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24603059-T-C

2299930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24603051-T-C

2299933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24603048-C-T

2299935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24603046-C-T

2299945-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24603037-G-C

2300045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24602975-T-C

2300066-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24602954-T-A

2300066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24602954-T-C

http://identifiers.org/hco/16/GRCh38#2300262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24602745-C-A

2303670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24601294-G-A

http://identifiers.org/hco/16/GRCh38#2303820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24601191-C-A

2303820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24601191-C-T

2303876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24601147-A-G

2304065-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 24600956-C-G

2304068-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 24600953-C-G

2304098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 24600923-G-A

2304098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24600923-G-C

2304424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24599016-T-C

2304495-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24598959-T-A

2304580-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24598860-C-G

2308405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24596883-G-A

2308427-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24596855-G-C

2308602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24596679-C-T

2316980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24596150-C-T

2317086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24596077-A-G

http://identifiers.org/hco/16/GRCh38#2317139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24596015-C-A

2317139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24596015-C-T

http://identifiers.org/hco/16/GRCh38#2317148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24596006-C-A

2317148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24596006-C-T

http://identifiers.org/hco/16/GRCh38#2317155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24595996-C-A

2317171-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24595980-T-G

2317234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24595851-G-T

http://identifiers.org/hco/16/GRCh38#2317267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24595779-C-A

2317267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24595779-C-T

2317522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24595557-T-C

2317522-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24595557-T-G

2317533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24595546-A-G

2317614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24595487-G-A

2317623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24595478-A-G

2317757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24595343-A-G

2318211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24594414-G-A

2318214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24594411-A-G

http://identifiers.org/hco/16/GRCh38#2318229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24594396-C-A

2318303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24594299-C-T

2318383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24594216-G-A

2319221-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24593890-C-G

2319523-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24593530-T-A

2319523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24593530-T-C

2319554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24593500-T-C

2319569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24593484-G-A

2319569-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24593484-G-C

2319630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24593426-G-A

2319630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24593426-G-T

2319636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24593420-T-C

2319636-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24593420-T-G

2319683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 24593373-C-T

2319870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24593191-C-T

2319882-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24593179-C-G

2319882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24593179-C-T

2319928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24593122-G-A

2319928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24593122-G-T

2319933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24593117-G-A

2319933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24593117-G-T

2319963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24593075-G-T

2319998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24593031-G-A

2320107-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24592947-T-A

http://identifiers.org/hco/16/GRCh38#2323585-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24585843-A-C

2323585-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24585843-A-T

2323713-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24585714-C-G

2323718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24585709-C-T

2323719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24585708-C-T

http://identifiers.org/hco/16/GRCh38#2323831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24585673-C-A

2323831-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24585673-C-G

2323831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24585673-C-T

http://identifiers.org/hco/16/GRCh38#2323835-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24585669-A-C

2323835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24585669-A-G

2323929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24585624-T-C

2324077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24585495-T-C

2324141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24585432-G-A

2324236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24585334-G-A

http://identifiers.org/hco/16/GRCh38#2324260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24585317-C-A

2324260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24585317-C-T

http://identifiers.org/hco/16/GRCh38#2324273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24585299-C-A

2324308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24585267-G-A

2324308-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24585267-G-C

2324308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24585267-G-T

2324344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24585236-G-A

2324344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24585236-G-T

2324371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24585211-G-A

2324371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24585211-G-T

2324380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24585204-G-A

2324380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24585204-G-T

http://identifiers.org/hco/16/GRCh38#2324388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24585198-C-A

2324388-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24585198-C-G

2324388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24585198-C-T

http://identifiers.org/hco/16/GRCh38#2324391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24585195-C-A

2324391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24585195-C-T

http://identifiers.org/hco/16/GRCh38#2324404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24585185-C-A

2324404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 24585185-C-T

2324592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24584999-G-A

2324592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24584999-G-T

http://identifiers.org/hco/16/GRCh38#2324649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24584934-C-A

2324649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24584934-C-T

2324680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24584909-T-C

2324737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24584850-C-T

http://identifiers.org/hco/16/GRCh38#2325132-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24584340-A-C

2325133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24584339-G-A

2325133-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24584339-G-C

2325142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24584330-C-T

2325179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24584298-C-T

2326039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24583900-A-G

2326040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24583899-C-T

2326065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 24583874-G-A

2326065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24583874-G-T

2326096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24583843-C-G

2326348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24583617-A-G

2326393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24583580-C-T

2326408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24583563-C-T

2326486-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24583493-C-G

2326486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24583493-C-T

http://identifiers.org/hco/16/GRCh38#2326571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24583399-C-A

2326571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24583399-C-T

http://identifiers.org/hco/16/GRCh38#2326622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24583349-C-A

2326622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24583349-C-T

2327130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24582929-T-C

2327238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24582830-G-A

2327255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24582814-G-A

2327255-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24582814-G-C

2327542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24582518-G-A

2327542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24582518-G-T

2327575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24582485-C-T

2327645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24582421-G-A

2327727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24582336-C-T

2328087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24582157-T-C

2328087-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24582157-T-G

2328521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24581938-G-A

2328521-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24581938-G-C

2328523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24581936-G-T

2328561-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24581915-A-T

2328653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24581855-G-A

http://identifiers.org/hco/16/GRCh38#2328692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24581817-C-A

2328692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24581817-C-T

http://identifiers.org/hco/16/GRCh38#2328711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24581799-C-A

2328740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24581762-T-C

http://identifiers.org/hco/16/GRCh38#2328744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24581758-C-A

2328744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24581758-C-T

2328762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24581740-T-C

2328768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24581734-C-T

2329334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24580560-T-C

2329334-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24580560-T-G

2329371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24580526-G-T

2329394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24580513-C-T

2329395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24580512-A-G

2329453-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24580459-T-G

2329547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24580152-C-T

2329585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24580114-A-G

2329585-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24580114-A-T

2329612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24580097-C-T

http://identifiers.org/hco/16/GRCh38#2329622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24580087-C-A

2329622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24580087-C-T

http://identifiers.org/hco/16/GRCh38#2329703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24580009-C-A

2329703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24580009-C-T

2329712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24580000-A-G

2329789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24579925-G-T

2331546-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24579234-C-G

2331546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24579234-C-T

2331775-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24579021-A-T

2332079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24578733-A-G

http://identifiers.org/hco/16/GRCh38#2332162-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24578648-A-C

http://identifiers.org/hco/16/GRCh38#2332199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24578622-C-A

2333516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24578150-G-A

2333984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

2333984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-T

2334215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

2338203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24573328-G-A

2338203-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24573328-G-C

2338353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24573209-T-C

2338432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24573118-T-C

2338500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24573053-C-T

2338544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24573023-G-C

2338570-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24573003-G-C

2338805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24572834-A-G

http://identifiers.org/hco/16/GRCh38#2339203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24572466-C-A

2339203-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24572466-C-G

2339320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24572349-G-T

2339336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24572333-G-A

2339451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24572257-T-C

2339853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24571820-G-A

2340118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24571582-C-T

2340300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24571440-C-T

2340428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24571350-G-A

2340428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24571350-G-T

http://identifiers.org/hco/16/GRCh38#2340586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24571210-C-A

2340586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24571210-C-T

2340588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24571208-G-C

2340588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24571208-G-T

2340636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24571162-G-A

2340636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24571162-G-T

2340704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24571091-G-A

2340704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24571091-G-T