73308353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100581248-G-A

73308353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100581248-G-T

http://identifiers.org/hco/11/GRCh38#73308467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100581135-C-A

73308467-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100581135-C-G

73308467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100581135-C-T

73308503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100581099-C-T

73308539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 100581063-T-C

73308575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100581009-G-A

73308575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100581009-G-T

http://identifiers.org/hco/11/GRCh38#73308657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100580926-C-A

73308657-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 100580926-C-G

73308657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 100580926-C-T

73308733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100580850-A-G

73308733-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100580850-A-T

73308862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100580721-T-C

73308862-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100580721-T-G

73308879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100580704-T-C

http://identifiers.org/hco/11/GRCh38#73308953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100580630-C-A

73308953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100580630-C-T

http://identifiers.org/hco/11/GRCh38#73308960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100580623-C-A

73308960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100580623-C-T

73308987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100580596-G-A

73308987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100580596-G-T

http://identifiers.org/hco/11/GRCh38#73309087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#100580496-C-A

73309087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 100580496-C-T

73309473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: 100580113-G-A

73309473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: 100580113-G-T

73309480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: 100580106-G-A

73309480-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: 100580106-G-C

73309480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: 100580106-G-T

73309513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: 100580073-G-A

73309513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: 100580073-G-T

73309549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense_variant, undefined
orthologous variants: 100580040-A-G

73309569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: 100580020-G-A

73309630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: 100579959-C-T

73309683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: 100579918-C-T

73310013-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: 100579585-C-G

73310013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: 100579585-C-T

73310190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: stop gained
orthologous variants: 100579417-G-T

73310196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: 100579411-A-G

73310391-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: 100579216-C-G

73310391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: 100579216-C-T

73310474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: synonymous variant
orthologous variants: 100579133-A-G

73310607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: 100579000-G-A

73310663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: synonymous variant
orthologous variants: 100578944-G-A

73310685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: 100578919-C-T

73310737-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: 100578867-C-G

73310737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: 100578867-C-T

73310778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: 100578826-C-T

73310866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: 100578738-G-A

73310866-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: 100578738-G-C

73311058-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: 100578546-C-G

73311088-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: 100578516-G-C

73311303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: synonymous variant
orthologous variants: 100578301-C-T

73311315-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: 100578292-C-G

73311315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: synonymous variant
orthologous variants: 100578292-C-T

73311475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: 100578132-G-T

http://identifiers.org/hco/11/GRCh38#73311552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100578055-C-A

73311552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: 100578055-C-T

73311579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: 100578028-C-T

73311588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: 100578019-G-T

73311621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: 100577986-C-T

73311800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: synonymous variant
orthologous variants: 100577804-T-C

http://identifiers.org/hco/11/GRCh38#73311863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100577743-C-A

73311863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100577743-C-T

73311878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100577728-G-A

73311920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100577694-G-T

73312126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100577537-C-G

73312187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100577463-A-G

73312288-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100577389-C-G

73312288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100577389-C-T

73312376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100577340-T-C

73312474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100577235-T-C

73312474-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100577235-T-G

73312811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100576923-C-T

73312835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100576915-C-T

73312995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100576749-T-C

73313129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100576616-C-T

73313155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100576592-C-T

73313279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100576471-G-A

73313293-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100576457-C-G

73313446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100576364-G-A

73313532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100576289-C-T

73313667-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100576181-G-C

73313722-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100576113-A-T

73313823-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100576034-T-A

73313996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100575862-G-T

73314018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100575840-A-G

73314123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100575735-G-A

73314188-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100575666-C-G

73314688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100575185-G-T

73314693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100575181-T-C

73314723-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100575161-T-G

73314726-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100575157-C-G

73315561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100574311-T-C

73315742-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100574141-C-G

73315940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100573944-C-T

73316052-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100573866-C-G

73316052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100573866-C-T

73316151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100573774-G-A

73316162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100573763-A-G

73316319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100573631-C-T

73316762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100573226-T-C

73317098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100572806-G-A

73317198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100572610-G-A

73317256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100572543-T-C

73317256-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100572543-T-G

http://identifiers.org/hco/11/GRCh38#73317595-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100572251-A-C

73317738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100572129-T-C

73318192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100571718-G-C

73318744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100571295-G-T

73318968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100571094-C-T

73319042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100571014-C-T

73319813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100570734-G-A

73319851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100570696-G-A

73319926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100570620-G-A

73321381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100569688-T-C

73321517-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100569575-C-G

73321544-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100569548-C-G

73321573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100569522-A-G

73321573-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100569522-A-T

73321629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100569467-A-G

73321648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100569448-C-T

73322258-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100568893-A-T

http://identifiers.org/hco/11/GRCh38#73322499-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100568701-A-C

73323802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100567419-G-T

73323808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100567413-G-A

73323936-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100567269-T-G

73324169-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100567113-T-G

73324207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100567086-G-A

73324225-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100567068-T-A

73324237-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100567056-C-G

http://identifiers.org/hco/11/GRCh38#73324351-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100566957-A-C

73324951-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100566093-C-G

73324956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100566088-G-A

73325280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100565790-A-G

73325322-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100565718-T-G

73325605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100565488-C-T

73325624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100565474-G-A

73325624-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100565474-G-C

73325895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100565186-G-A

http://identifiers.org/hco/11/GRCh38#73325984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100565027-C-A

73326066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100564952-C-T

73326290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100564814-G-A

73326382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100564722-G-A

73326784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100564633-A-G

73326834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100564582-G-T

73326966-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100564457-G-C

73326992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100564446-C-T

http://identifiers.org/hco/11/GRCh38#73328189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100563507-C-A

http://identifiers.org/hco/11/GRCh38#73328199-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100563497-A-C

http://identifiers.org/hco/11/GRCh38#73328332-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100563364-A-C

73328593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100563122-G-C

73330376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100561731-C-T

73330687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100561414-T-C

73331230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, undefined
orthologous variants: 100560893-G-A

73331230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, undefined
orthologous variants: 100560893-G-C

73331696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100560490-A-G

73331711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100560475-C-T

73332074-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100560096-A-T

73332080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100560090-T-C

73332301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100559866-C-T

73332419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100559776-A-G

73332523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100559667-C-T

73332601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100559615-G-A

73332833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100559422-G-A

73332971-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100559286-G-C

73333000-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100559252-G-C

73333297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100558974-A-G

73333315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100558956-C-T

73333405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100558912-C-T

73333486-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100558837-G-C

73333618-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100558715-G-C

73333701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100558664-G-A

73333728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100558642-C-T

73333741-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100558629-C-G

73333825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100558406-C-T

73333918-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100558127-G-C

73334131-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100557937-G-C

73334340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100557752-G-T

73334460-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100557703-G-C

73334491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100557680-C-T

73334709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100557474-A-G

73334761-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100557418-C-G

73334942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100557212-C-T

73334972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100557162-C-T

73335122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100557029-G-A

73335388-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 100556857-C-G

73335474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 100556783-T-C

73335497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100556760-G-A

http://identifiers.org/hco/11/GRCh38#73335610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#100556648-C-A

73336057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100556279-C-T

73336364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100555926-A-G

73336375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100555912-A-G

73336385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100555904-C-T

73336619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100555671-T-C

73336675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100555618-G-A

73336792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100555517-G-C

73337279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100555089-G-A

http://identifiers.org/hco/11/GRCh38#73337281-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100555087-A-C

73337299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100555069-C-T

73338013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100554038-A-G

73338246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100553846-A-G

73338483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100553622-G-A

73339316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100551996-A-G

73339579-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100551779-G-C

73339684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100551687-G-A

73339942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100551349-T-C

73340437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100546978-T-C

73340879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100546654-G-T

73340946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100546588-A-G

73341676-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100544946-C-G

73341694-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100544929-T-G

73341719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, undefined
orthologous variants: 100544910-G-A

73341899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100544735-G-A

73341944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100544701-T-C

73342005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100544639-G-A

73342155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100544532-G-A

73342156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100544531-G-A

73342174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100544526-G-A

73342176-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100544524-T-G

73342433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100544301-G-A

73342439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100544295-G-C

73342439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100544295-G-T

73342776-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, undefined
orthologous variants: 100544044-G-C

http://identifiers.org/hco/11/GRCh38#73342832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100544027-C-A

73342832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100544027-C-T

http://identifiers.org/hco/11/GRCh38#73343005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100543892-C-A

73343005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100543892-C-T

73343025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100543878-G-A

http://identifiers.org/hco/11/GRCh38#73343067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100543835-C-A

73343067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100543835-C-T

http://identifiers.org/hco/11/GRCh38#73343185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100543749-C-A

73343233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100543701-G-A

73343233-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100543701-G-C

73343233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100543701-G-T

http://identifiers.org/hco/11/GRCh38#73343234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100543700-C-A

73343234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100543700-C-T

73343282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100543643-G-A

73343282-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100543643-G-C

73343282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100543643-G-T

73343327-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100543598-T-A

73343327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100543598-T-C

73343379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100543538-G-A

73343379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100543538-G-T

http://identifiers.org/hco/11/GRCh38#73343398-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100543504-A-C

73343398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100543504-A-G

73343955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100542994-G-T

http://identifiers.org/hco/11/GRCh38#73343996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100542957-C-A

73344089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100542887-G-A

73344295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100542689-A-G

73344304-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100542680-C-G

73344304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100542680-C-T

73344305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100542679-G-A

73344305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100542679-G-T

73344379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100542606-C-G

73344379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100542606-C-T

73344795-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100542207-G-C

73345022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100542004-C-T

73345052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100541974-C-T

73345202-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100541907-C-G

73345316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100541833-G-A

73345362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100541793-G-T

73345602-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100541553-C-G

73345641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100541513-T-C

http://identifiers.org/hco/11/GRCh38#73345677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100541477-C-A

73345706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100541449-A-G

73345912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100541327-G-C

http://identifiers.org/hco/11/GRCh38#73346229-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100540282-A-C

73346493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100540058-G-A

73346604-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100539940-T-A

73346752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100539844-G-A

73346752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100539844-G-T

73346808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100539780-G-T

http://identifiers.org/hco/11/GRCh38#73346877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100539709-C-A

73346877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 100539709-C-T

http://identifiers.org/hco/11/GRCh38#73346925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100539661-C-A

73347008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 100539583-G-A

73347049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 100539552-A-G

73347190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 100539463-G-A

73347190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 100539463-G-T

73347309-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100539381-T-A

73347309-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100539381-T-G

73347610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100538948-C-T

73347612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100538946-C-T

73347789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100538770-T-C

http://identifiers.org/hco/11/GRCh38#73347829-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100538726-A-C

73348151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100538421-G-A

73348210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100538400-C-T

73348386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100538188-G-A

http://identifiers.org/hco/11/GRCh38#73348508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100538082-C-A

73348637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100537950-G-A

73348688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100537782-G-A

73348697-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100537773-C-G

73348716-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100537703-G-C

73348840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100537553-A-G

73348840-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100537553-A-T

73348994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100537400-G-A

73349004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100537391-A-G

73349198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100537244-A-G

73349212-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100537211-T-G

73350061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

73351119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100536209-C-T

http://identifiers.org/hco/11/GRCh38#73351388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#100535924-C-A

73351388-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100535924-C-G

73352518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100535380-G-A

73352592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100535299-T-C

73352687-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100535201-T-G

73352702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100535186-G-A

73352702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100535186-G-T

73352704-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100535184-T-G

73352705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100535183-G-A

73352705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100535183-G-T

73352730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100535159-G-T

73352917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100534977-C-T

73354077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100534071-G-A

73354102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100534042-T-C

73354108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100534036-G-A

73355957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100532671-G-A

73355995-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100532637-G-C

73356002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100532630-G-A

73356002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100532630-G-T

73356141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100532522-A-G

73356229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: 100532443-G-A

73356307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: 100532365-C-T

http://identifiers.org/hco/11/GRCh38#73356542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100532166-C-A

73356660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100532062-A-G

73356909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100531840-G-A

73356936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100531812-G-T

73356973-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100531776-T-G

http://identifiers.org/hco/11/GRCh38#73356994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100531755-C-A

73357255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: 100531497-A-G

73357405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100531375-G-T

73357408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100531372-T-C

http://identifiers.org/hco/11/GRCh38#73357447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100531334-C-A

73357447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100531334-C-T

73359609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100531230-C-T

http://identifiers.org/hco/11/GRCh38#73359708-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100531135-A-C

73359708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100531135-A-G

73359708-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100531135-A-T

73359709-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100531134-T-A

73359709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100531134-T-C

73359727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100531116-T-C

73359729-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100531114-T-A

73359729-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100531114-T-G

73359754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100531089-G-A

73359754-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100531089-G-C

73359754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100531089-G-T

http://identifiers.org/hco/11/GRCh38#73359793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100531051-C-A

73359793-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100531051-C-G

73359807-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100531044-G-C

73359861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: 100530989-A-G

73359869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: 100530981-A-G

73360053-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100530803-T-A

73360053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100530803-T-C

73360085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100530771-G-T

73360165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100530704-A-G

73360204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100530686-G-A

73360204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100530686-G-T

73360231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100530665-A-G

73360260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100530653-G-A

73360260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100530653-G-C

http://identifiers.org/hco/11/GRCh38#73360263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100530650-C-A

73360263-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100530650-C-G

73360347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: 100530570-T-C

73360549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100530368-T-C

73360549-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100530368-T-G

73360566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100530352-T-C

73360648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, undefined
orthologous variants: 100530288-G-A

73360648-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, undefined
orthologous variants: 100530288-G-C

73360648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, undefined
orthologous variants: 100530288-G-T

73360939-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100530022-C-G

73360939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100530022-C-T

http://identifiers.org/hco/11/GRCh38#73360966-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100529980-A-C

73360966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100529980-A-G

http://identifiers.org/hco/11/GRCh38#73361010-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100529958-A-C

73361351-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100529689-T-G

http://identifiers.org/hco/11/GRCh38#73361925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#100529438-C-A

73361925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, undefined
orthologous variants: 100529438-C-T

http://identifiers.org/hco/11/GRCh38#73361954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#100529408-C-A

73362109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense_variant, undefined
orthologous variants: 100529268-G-A

73362235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: 100529142-C-T

http://identifiers.org/hco/11/GRCh38#73362236-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100529141-A-C

73362236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: 100529141-A-G

http://identifiers.org/hco/11/GRCh38#73362264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100529117-C-A

73362264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100529117-C-T

73362266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100529115-G-A

73362332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100529063-G-T

73362333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100529062-G-A

73362333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100529062-G-T

73362348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100529039-G-T

73362381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100529007-G-A

73362381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100529007-G-T

73362382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100529006-G-A

73362382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100529006-G-T

http://identifiers.org/hco/11/GRCh38#73362410-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100528984-A-C

73362410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100528984-A-G

73362410-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100528984-A-T

http://identifiers.org/hco/11/GRCh38#73362417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100528977-C-A

73362417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100528977-C-T

73362425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 100528969-T-C

73362452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: 100528942-A-G

73362455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: 100528939-A-G

73362530-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: 100528864-A-T

73362608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: 100528783-G-A

73362608-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: 100528783-G-C

73362608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: 100528783-G-T

73362659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: 100528732-G-A

73362659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: 100528732-G-T

73362731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: 100528660-G-T

73362744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100528647-G-A

73362744-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100528647-G-C

73362744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100528647-G-T

http://identifiers.org/hco/11/GRCh38#73363080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100528370-C-A

73363080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100528370-C-T

73363119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100528345-T-C

73363244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: 100528221-A-G

73363256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: stop gained
orthologous variants: 100528209-G-T

http://identifiers.org/hco/11/GRCh38#73363392-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100528073-A-C

73363540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100527974-G-A

73363540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100527974-G-T

http://identifiers.org/hco/11/GRCh38#73363562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100527954-C-A

73363562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100527954-C-T

73363593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100527923-G-A

73363595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100527921-G-A

73363610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100527907-G-T

73363662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100527873-G-A

73363662-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100527873-G-C

73363662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100527873-G-T

73363763-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: 100527769-T-G

73363826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense variant
orthologous variants: 100527706-T-C

http://identifiers.org/hco/11/GRCh38#73363866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100527667-C-A

73363866-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100527667-C-G

73363887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100527647-G-A

73363887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100527647-G-T

73363949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100527589-G-A

http://identifiers.org/hco/11/GRCh38#73363962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100527576-C-A

73363962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100527576-C-T

http://identifiers.org/hco/11/GRCh38#73363973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100527565-C-A

http://identifiers.org/hco/11/GRCh38#73363985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100527553-C-A

73363985-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100527553-C-G

73363985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100527553-C-T

http://identifiers.org/hco/11/GRCh38#73364034-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100527506-A-C

73364034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100527506-A-G

http://identifiers.org/hco/11/GRCh38#73364039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100527501-C-A

73364039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100527501-C-T

73364061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100527473-A-G

73364061-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100527473-A-T

http://identifiers.org/hco/11/GRCh38#73364071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100527463-C-A

73364071-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100527463-C-G

73364073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100527461-C-T

http://identifiers.org/hco/11/GRCh38#73364112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100527423-C-A

73364112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100527423-C-T

http://identifiers.org/hco/11/GRCh38#73364113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100527422-C-A

73364113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100527422-C-G

73364144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100527390-C-T

http://identifiers.org/hco/11/GRCh38#73364263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100527285-C-A

73364310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100527204-T-C

73364323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100527191-C-T

73364428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100527097-C-T

http://identifiers.org/hco/11/GRCh38#73364538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100526975-C-A

73364538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100526975-C-T

73364640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100526874-G-T

http://identifiers.org/hco/11/GRCh38#73364723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100526795-C-A

73364723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100526795-C-T

http://identifiers.org/hco/11/GRCh38#73364820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100526697-C-A

73364820-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100526697-C-G

73364820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100526697-C-T

73364835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100526682-G-A

73364835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100526682-G-T

73364919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100526614-A-G

http://identifiers.org/hco/11/GRCh38#73365064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100526492-C-A

73365064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100526492-C-T

http://identifiers.org/hco/11/GRCh38#73365110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100526433-C-A

http://identifiers.org/hco/11/GRCh38#73365135-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100526408-A-C

73365135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron variant
orthologous variants: 100526408-A-G

73365418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100526117-G-A

http://identifiers.org/hco/11/GRCh38#73365516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100526019-C-A

73365570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100525965-G-A

73365672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 100525893-C-T

73365743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100525822-G-C

73365752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100525813-C-T

73366015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100525581-G-T

73366131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100525469-G-A

73366131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100525469-G-T

73366261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100525336-T-C

73366272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100525327-G-A

73367174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100525036-C-T

73367215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100524991-C-T

73367442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100522943-T-C

73367486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100522905-T-C

73367730-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100522655-A-T

73367829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 100522556-G-A

73367829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 100522556-G-T

73367897-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100522496-G-C

73367897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100522496-G-T

73367907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100522486-T-C

73367914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100522479-T-C

73367948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 3 prime UTR variant
orthologous variants: 100522446-G-A

73368100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 3 prime UTR variant
orthologous variants: 100522298-G-A

73368100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 3 prime UTR variant
orthologous variants: 100522298-G-T

73368154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 3 prime UTR variant
orthologous variants: 100522237-T-C

http://identifiers.org/hco/11/GRCh38#73368194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100522197-C-A

73368194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 3 prime UTR variant
orthologous variants: 100522197-C-T

73368239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 3 prime UTR variant
orthologous variants: 100522159-G-T

http://identifiers.org/hco/11/GRCh38#73368344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100522057-C-A

73368354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 3 prime UTR variant
orthologous variants: 100522044-T-C

73368354-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 3 prime UTR variant
orthologous variants: 100522044-T-G

73368369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 3 prime UTR variant
orthologous variants: 100522020-A-G

http://identifiers.org/hco/11/GRCh38#73368457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100521937-C-A

73368457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 3 prime UTR variant
orthologous variants: 100521937-C-T

http://identifiers.org/hco/11/GRCh38#73368473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100521919-C-A

73368473-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 3 prime UTR variant
orthologous variants: 100521919-C-G

73368473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 3 prime UTR variant
orthologous variants: 100521919-C-T

73368491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 3 prime UTR variant
orthologous variants: 100521917-T-C

73368512-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 3 prime UTR variant
orthologous variants: 100521895-T-A

73368512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 3 prime UTR variant
orthologous variants: 100521895-T-C

73368522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 3 prime UTR variant
orthologous variants: 100521885-T-C

73368522-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 3 prime UTR variant
orthologous variants: 100521885-T-G

73368561-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 3 prime UTR variant
orthologous variants: 100521856-T-A

http://identifiers.org/hco/11/GRCh38#73368641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100521781-C-A

http://identifiers.org/hco/11/GRCh38#73368710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100521716-C-A

73368745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 3 prime UTR variant
orthologous variants: 100521667-A-G

73368769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 3 prime UTR variant
orthologous variants: 100521643-T-C

http://identifiers.org/hco/11/GRCh38#73368949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100521471-C-A

73368949-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 3 prime UTR variant
orthologous variants: 100521471-C-G

73368949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 3 prime UTR variant
orthologous variants: 100521471-C-T

http://identifiers.org/hco/11/GRCh38#73369164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100521261-C-A

73369175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 3 prime UTR variant
orthologous variants: 100521250-G-T

73369192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 3 prime UTR variant
orthologous variants: 100521233-G-T

73369242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 3 prime UTR variant
orthologous variants: 100521189-A-G

73369242-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 3 prime UTR variant
orthologous variants: 100521189-A-T

73369284-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 3 prime UTR variant
orthologous variants: 100521145-T-A

73369334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 3 prime UTR variant
orthologous variants: 100521123-A-G

http://identifiers.org/hco/11/GRCh38#73369342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100521115-C-A

73369342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 3 prime UTR variant
orthologous variants: 100521115-C-T

73369383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21726
most severe consequence: 3 prime UTR variant
orthologous variants: 100521095-T-C