18983986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 118183937-G-A

18983986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 118183937-G-T

18983991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 118183932-G-A

18983991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 118183932-G-T

18983999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 118183924-G-A

18983999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 118183924-G-T

18984003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 118183920-G-A

18984003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 118183920-G-T

http://identifiers.org/hco/16/GRCh38#18984031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#118183902-C-A

18984031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 118183902-C-T

18984034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 118183899-G-A

18984034-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 118183899-G-C

18984034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 118183899-G-T

18984035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 118183898-G-A

18984035-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 118183898-G-C

18984035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 118183898-G-T

http://identifiers.org/hco/16/GRCh38#18984090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118183864-C-A

18984090-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 118183864-C-G

18984090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 118183864-C-T

http://identifiers.org/hco/16/GRCh38#18984094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118183860-C-A

18984094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118183860-C-T

18984211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118183781-G-A

18984211-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118183781-G-C

18984211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118183781-G-T

18984283-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118183733-G-C

18984283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118183733-G-T

18984412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118183643-C-T

http://identifiers.org/hco/16/GRCh38#18984459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118183595-C-A

http://identifiers.org/hco/16/GRCh38#18984467-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118183587-A-C

18984535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118183548-C-T

18984562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118183523-T-C

18984622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118183470-G-A

18984622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118183470-G-T

18984701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118183416-G-T

18984806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118183308-C-T

18989090-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118178136-C-G

18989329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118177915-C-T

http://identifiers.org/hco/16/GRCh38#18989360-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#118177884-A-C

18989632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118177631-G-A

18998894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118173443-C-T

19001161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118171140-A-G

19001271-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118171031-G-C

19001280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118171022-C-T

19002074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118170218-A-G

http://identifiers.org/hco/16/GRCh38#19002163-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118170163-A-C

19002975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118169604-G-A

19005521-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118168749-A-T

19005622-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118168666-C-G

19005854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118168448-G-A

http://identifiers.org/hco/16/GRCh38#19005918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#118168402-C-A

19005918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118168402-C-T

19005922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118168398-A-G

19005935-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118168386-T-A

19006060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118168256-C-T

19007297-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118167601-C-G

19007297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118167601-C-T

19007398-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118167523-A-T

19007401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118167520-G-A

http://identifiers.org/hco/16/GRCh38#19007479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118167436-C-A

http://identifiers.org/hco/16/GRCh38#19007773-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118167235-A-C

19007829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118167170-C-T

19007946-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118167053-T-G

19007979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118167020-A-G

19008012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118166970-A-G

19009039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118165748-A-G

19009049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118165738-T-C

19009055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118165733-C-T

19009097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118165694-T-C

http://identifiers.org/hco/16/GRCh38#19009100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118165691-C-A

19009100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118165691-C-T

http://identifiers.org/hco/16/GRCh38#19009124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118165677-C-A

19009124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118165677-C-T

19009145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118165667-A-G

19009173-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 118165645-G-C

19009326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 118165495-C-T

19016420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118163636-G-T

19016493-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118163543-C-G

19016493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 118163543-C-T

19016608-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118163421-C-G

19016608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118163421-C-T

19019985-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118161171-T-G

19020034-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118161129-G-C

19020142-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118161050-T-A

19020163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118161029-A-G

19020207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118160994-T-C

19020385-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118160839-T-A

19021611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118160398-C-G

19021611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118160398-C-T

19021871-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118160171-T-A

19021871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118160171-T-C

http://identifiers.org/hco/16/GRCh38#19021891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118160151-C-A

19021891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118160151-C-T

19021896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118160146-G-A

19021915-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118160129-T-A

19023193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 118158079-A-G

19023193-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 118158079-A-T

19025669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118157651-C-T

19030089-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118155286-G-C

19030145-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118155241-T-A

19030189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118155222-A-G

19030326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118155087-A-G

19030329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118155084-A-G

19030338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 118155075-C-T

http://identifiers.org/hco/16/GRCh38#19030472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118153917-C-A

19030472-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118153917-C-G

19030520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118153875-A-G

19030520-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118153875-A-T

19031023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118153671-C-T

19031114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118153585-G-A

19031121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118153578-A-G

19031187-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118153517-C-G

19035583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118152154-A-G

19035621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118152116-G-T

19035710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118152032-A-G

19035716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 118152026-G-T

19035819-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 118151923-T-G

19035848-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118151876-G-C

19035848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118151876-G-T

19035873-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118151851-T-A

19035900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118151826-G-T

http://identifiers.org/hco/16/GRCh38#19037944-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118150460-A-C

http://identifiers.org/hco/16/GRCh38#19037952-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118150452-A-C

19040179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118149445-A-G

19040179-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118149445-A-T

http://identifiers.org/hco/16/GRCh38#19040204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118149394-C-A

19040468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118149142-G-A

19040468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118149142-G-T

19040641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118148983-A-G

19040764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118148854-A-G

19044848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118146970-C-T

http://identifiers.org/hco/16/GRCh38#19045143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118146781-C-A

19045143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118146781-C-T

19045174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118146760-G-T

http://identifiers.org/hco/16/GRCh38#19045190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118146744-C-A

19045190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118146744-C-T

19045216-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118146729-A-T

http://identifiers.org/hco/16/GRCh38#19045267-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118146695-A-C

19045268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118146694-A-G

19045404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 118146572-T-C

http://identifiers.org/hco/16/GRCh38#19045446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118146530-C-A

19045446-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 118146530-C-G

19045446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 118146530-C-T

19045449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118146527-G-A

19045449-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118146527-G-C

19045449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118146527-G-T

19045454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118146525-G-A

19045458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118146521-A-G

19045460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118146519-A-G

http://identifiers.org/hco/16/GRCh38#19045468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118146511-C-A

19047006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118145071-A-G

19047006-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118145071-A-T

19047007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118145070-T-C

19047154-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118144918-T-A

19047502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118144516-A-G

http://identifiers.org/hco/16/GRCh38#19049547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118143500-C-A

19049547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118143500-C-T

19049652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118143435-A-G

http://identifiers.org/hco/16/GRCh38#19049721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118143385-C-A

19049763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118143361-C-T

19049806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118143328-C-T

19049812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118143322-T-C

19049885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118143259-A-G

19050016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118143139-G-T

http://identifiers.org/hco/16/GRCh38#19051717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118142619-C-A

19056118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118141600-T-C

19056119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118141599-T-C

19056120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118141598-G-T

19056122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118141596-C-T

19056176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118141559-G-A

19056427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118141352-A-G

19056430-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118141349-T-G

19056531-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118141272-T-G

19056588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 118141216-A-G

19056652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 118141152-G-A

19056652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 118141152-G-T

19056720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118141077-C-T

19057334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118139810-G-T

http://identifiers.org/hco/16/GRCh38#19057487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118139665-C-A

19057488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118139664-A-G

19057869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118139304-C-T

19057925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118139256-A-G

19059465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118138665-G-T

19061630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118137609-G-A

19061630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118137609-G-T

http://identifiers.org/hco/16/GRCh38#19061634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118137605-C-A

19061634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118137605-C-T

19061637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118137602-T-C

http://identifiers.org/hco/16/GRCh38#19061646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118137586-C-A

19061646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118137586-C-T

19061651-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118137581-T-A

19061724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118137496-A-G

19061725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118137495-T-C

19061869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 118137350-G-A

19061872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 118137347-T-C

19061872-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 118137347-T-G

http://identifiers.org/hco/16/GRCh38#19061917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118137307-C-A

19062678-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118136295-T-A

http://identifiers.org/hco/16/GRCh38#19062804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118136206-C-A

19062956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118136096-G-A

19063689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118135592-T-C

19063781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118135507-G-T

http://identifiers.org/hco/16/GRCh38#19063893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23000
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#118135411-C-A