181064399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: non coding transcript exon variant
orthologous variants: 50370106-C-T

181064410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: non coding transcript exon variant
orthologous variants: 50370097-G-A

181064410-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: non coding transcript exon variant
orthologous variants: 50370097-G-C

181064457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: non coding transcript exon variant
orthologous variants: 50370054-T-C

181064553-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50369943-T-A

181064724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50369764-G-A

181064740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50369748-A-G

181064981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50369509-C-T

181065008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50369482-A-G

181065083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50369406-A-G

181065496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50368997-T-C

181065538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50368957-T-C

181065572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50368924-T-C

http://identifiers.org/hco/4/GRCh38#181065589-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#50368907-A-C

181065589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50368907-A-G

181065781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50368643-A-G

http://identifiers.org/hco/4/GRCh38#181065990-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#50368439-A-C

181066024-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50368407-C-G

181066024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50368407-C-T

http://identifiers.org/hco/4/GRCh38#181068597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#50365031-C-A

181068597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50365031-C-T

http://identifiers.org/hco/4/GRCh38#181068770-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#50364844-A-C

181068770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50364844-A-G

181069333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50364133-C-T

181069463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50363995-G-T

181070821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50362059-T-C

181070846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50362039-A-G

181070931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50361953-G-A

181071204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50361618-G-A

181071204-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50361618-G-C

181071606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50361232-G-A

181071649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50361188-A-G

181071667-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50361170-T-G

181071672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50361165-A-G

181071672-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50361165-A-T

181072212-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50360919-G-C

181072212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50360919-G-T

181072227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50360904-C-T

181072398-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50360728-T-A

181072474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50360655-A-G

181072492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50360638-A-G

181072865-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50360371-T-A

181072872-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50360364-T-A

181073484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50359296-A-G

http://identifiers.org/hco/4/GRCh38#181073770-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#50359040-A-C

181073770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50359040-A-G

181075123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50358704-C-T

181075281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50358385-T-C

181075688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50357984-G-A

181075859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50357807-T-C

181076081-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50357586-T-G

181076094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50357573-A-G

181076736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50356676-T-C

http://identifiers.org/hco/4/GRCh38#181076751-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#50356661-A-C

181076751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50356661-A-G

181076837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50356426-C-T

http://identifiers.org/hco/4/GRCh38#181076843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#50356420-C-A

181076962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50356254-A-G

181076992-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50356220-A-T

181077053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50356158-A-G

181077174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50356039-G-A

181077348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50355863-C-T

181077354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50355857-T-C

181077426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50355739-G-A

http://identifiers.org/hco/4/GRCh38#181077453-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#50355713-A-C

181077915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50355255-C-T

181077939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50355231-A-G

181078012-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50355135-T-A

181078080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50355051-C-T

181079256-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50353842-T-G

181079308-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50353371-A-T

181079824-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50352444-T-A

http://identifiers.org/hco/4/GRCh38#181079825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#50352443-C-A

181079825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50352443-C-T

181079831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50352437-C-T

181079873-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50352357-A-T

181079891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50352339-G-A

181079923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50352308-C-T

181079931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50352300-G-A

181079931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50352300-G-T

181079993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50352250-A-G

181083524-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50351050-C-G

181083524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50351050-C-T

181083565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50351008-C-T

181083577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50350995-G-A

181083722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50350842-T-C

181084227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50350524-G-A

181084547-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50350208-A-T

181084639-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50350119-T-A

181084799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50349959-T-C

181084845-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50349911-T-A

181084946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50349814-G-T

181085105-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50349678-G-C

181085342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50349467-A-G

181085391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50349420-G-A

181085404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50349414-C-T

181085443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50349387-C-T

http://identifiers.org/hco/4/GRCh38#181085486-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#50349347-A-C

181085486-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50349347-A-T

181085864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50348997-A-G

181086179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50348718-G-A

181086183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50348714-C-T

181086187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50348710-T-C

181086217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50348680-G-A

181086267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50348631-A-G

181087401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50347975-T-C

http://identifiers.org/hco/4/GRCh38#181087647-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#50347761-A-C

181088021-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50347469-T-G

181093282-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50345550-T-G

181093324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50345508-A-G

181093356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50345480-C-T

181095754-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50345183-G-C

181095939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50345029-C-T

181096009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50344958-T-C

181096284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50344675-A-G

181096537-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50344385-C-G

181096596-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50344334-A-T

181096601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50344329-A-G

181096607-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50344323-C-G

181096628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50344301-A-G

181096856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50344077-G-A

181097053-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50343890-T-G

181097066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50343877-A-G

181097086-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50343857-G-C

181097086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50343857-G-T

181097384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50343570-G-T

181097450-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50343508-A-T

181097553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50343414-G-A

181097609-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50343348-T-A

181097609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50343348-T-C

181097723-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50343227-T-G

http://identifiers.org/hco/4/GRCh38#181097766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#50343183-C-A

181098161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50342794-G-A

181098325-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50342645-C-G

181098325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50342645-C-T

181098371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50342610-G-A

181098390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50342584-A-G

181098438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50342537-C-T

181099538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50341035-C-T

181099580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50340994-A-G

181099634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50340940-G-T

181099800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50340785-G-A

http://identifiers.org/hco/4/GRCh38#181099817-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#50340768-A-C

181099817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50340768-A-G

181099869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50340716-A-G

181099869-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50340716-A-T

181099895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50340696-G-A

181099895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50340696-G-T

181100004-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50340595-A-T

181100086-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50340517-T-G

181100187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50340419-G-A

181100215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50340391-G-A

181100230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50340370-C-T

http://identifiers.org/hco/4/GRCh38#181100468-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#50340148-A-C

181100550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50340078-T-C

181100642-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50339984-T-A

181100807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50339792-G-A

181100823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50339776-G-T

181101222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50339377-C-T

181101233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50339366-T-C

181101327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50339269-A-G

181101381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50339218-T-C

181101392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50339207-C-T

181101438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50339161-C-T

http://identifiers.org/hco/4/GRCh38#181101546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#50339059-C-A

181101562-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50339043-T-G

181101740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50338735-A-G

181101754-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50338729-T-A

181101830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50338653-A-G

181101868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50338619-T-C

181102061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50338434-A-G

181102129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50338359-A-G

181102436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50338087-A-G

181102518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50338050-C-G

181103028-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50337821-T-A

181103028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50337821-T-C

181103179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50337690-A-G

181103435-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50337331-T-A

181103549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50337203-G-A

181103591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50337161-A-G

181103939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50336862-C-T

181104023-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50336789-T-G

http://identifiers.org/hco/4/GRCh38#181104260-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#50336563-A-C

181104381-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50336445-C-G

181104414-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50336412-C-G

181104706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50336118-A-G

http://identifiers.org/hco/4/GRCh38#181104753-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#50336063-A-C

181104753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50336063-A-G

181104843-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50335966-T-A

http://identifiers.org/hco/4/GRCh38#181104850-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#50335959-A-C

181104930-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50335887-T-G

181105250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50335551-G-A

181105293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50335504-A-G

http://identifiers.org/hco/4/GRCh38#181105448-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#50335327-A-C

181105461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50335314-G-A

181105635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50335136-T-C

181105798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50334971-T-C

181105874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50334893-A-G

181106357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50334413-A-G

181106442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50334334-T-C

181106478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50334293-A-G

181106545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50334240-C-T

181106667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50333967-A-G

181106808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50333769-G-A

181106834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50333745-T-C

181106858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50333675-T-C

181107100-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50333298-C-G

181107100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50333298-C-T

181107421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50333025-G-A

181107823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50332375-A-G

181109000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50323915-A-G

181109011-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50323907-C-G

181110290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50322551-T-C

181110313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50322528-G-A

181110480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50322418-C-T

181118437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50320416-A-G

http://identifiers.org/hco/4/GRCh38#181118474-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#50320383-A-C

181118498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50320359-T-C

181118498-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50320359-T-G

181118516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50320341-T-C

181118794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50319899-G-A

181118871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50319815-A-G

181118953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50319735-C-T

181119574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50319147-T-C

181119579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50319142-G-A

181119780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50318732-C-T

http://identifiers.org/hco/4/GRCh38#181119874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#50318638-C-A

181119874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50318638-C-T

181119929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50318577-C-T

181120756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50318101-G-T

181121176-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50317731-A-T

181121198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50317703-A-G

181121673-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50317270-A-T

181122047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50316897-G-A

181122284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50316654-G-A

181122372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50316573-A-G

181122843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50316149-G-A

181123296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50315467-C-T

181123386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50315376-G-A

181123553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50315214-A-G

http://identifiers.org/hco/4/GRCh38#181123675-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#50315085-A-C

181123918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50314174-G-A

181123918-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50314174-G-C

181123979-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50314119-T-A

http://identifiers.org/hco/4/GRCh38#181124003-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#50314098-A-C

181124063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50314038-A-G

181124180-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50313894-A-T

181124292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50313773-G-A

181124575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50313493-A-G

181125031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50306613-G-A

181125085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50306555-G-A

181125190-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50306459-T-A

181125305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50306381-G-A

181125363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50306325-T-C

181125394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50306297-G-A

181125877-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50306222-G-C

181125981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50306105-C-T

181125982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50306104-A-G

181126152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50305942-A-G

181126242-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50305861-C-G

181128241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50301206-A-G

181128341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50301107-A-G

181128346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50301102-G-A

181128758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50300553-C-T

181129039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50300035-G-A

181129039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50300035-G-T

181129041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50300033-C-T

181129097-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50299967-A-T

http://identifiers.org/hco/4/GRCh38#181131571-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#50299641-A-C

181131828-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50299280-T-G

181132502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50298490-A-G

181132649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50298357-T-C

181132727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50298280-A-G

181132796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50298217-T-C

181132837-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50298176-A-T

181132952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50298069-T-C

181133121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50297915-A-G

181133483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50297554-T-C

181133680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50297365-G-A

181133936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50297120-G-A

http://identifiers.org/hco/4/GRCh38#181134047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#50297015-C-A

181134047-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50297015-C-G

181134329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50296754-T-C

http://identifiers.org/hco/4/GRCh38#181134692-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#50296686-A-C

181134808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50296571-T-C

181135132-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50295499-C-G

181135134-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50295497-G-C

181135165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50295466-T-C

181135216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50295419-A-G

http://identifiers.org/hco/4/GRCh38#181135233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#50295414-C-A

181135429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50295199-A-G

181135540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50295076-G-T

181135640-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50294978-T-A

181135640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50294978-T-C

181135641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50294977-G-A

181137179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50294344-C-G

181137237-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50294276-A-T

181137253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50294260-T-C

181137298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50294224-G-T

181137311-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50294213-A-T

181137334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50294190-T-C

181137352-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50294172-T-A

181137508-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50293995-T-A

181137767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50293748-G-T

181137795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50293720-G-T

181138273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50287682-G-A

181138467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50287487-T-C

181138487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50287467-A-G

181138513-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50287440-T-G

181138584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50287382-C-T

181138955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50287008-G-A

181138955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50287008-G-T

181139010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50286952-G-T

181139192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50286761-A-G

181139192-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50286761-A-T

181139250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50286695-T-C

181139256-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50286689-A-T

181139484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50286480-C-T

181139641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50286322-T-C

181140327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50285265-C-T

181140680-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50284917-T-G

http://identifiers.org/hco/4/GRCh38#181140757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#50284843-C-A

181140757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50284843-C-T

181140871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50284728-A-G

http://identifiers.org/hco/4/GRCh38#181140880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#50284719-C-A

181140880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50284719-C-T

http://identifiers.org/hco/4/GRCh38#181140958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#50284628-C-A

181140987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50284600-T-C

181142022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50283793-C-T

181142046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50283769-A-G

181142657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50283276-A-G

http://identifiers.org/hco/4/GRCh38#181142840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#50283119-C-A

181142874-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50283092-C-G

181142891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50283080-T-C

181143171-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50282854-G-C

181143275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50282761-G-T

181143390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 50282644-A-G

181143414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 50282620-A-G

181143483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 50282553-A-G

181143580-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 50282456-T-A

181143632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50282404-T-C

181143814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50282232-T-C

http://identifiers.org/hco/4/GRCh38#181143947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#50282100-C-A

181143947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50282100-C-T

http://identifiers.org/hco/4/GRCh38#181144012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#50282036-C-A

181144404-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50281070-T-A

181144427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50281045-A-G

181144700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50280817-T-C

181144732-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50280777-T-A

181144732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50280777-T-C

181144777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50280732-G-A

181145227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50280511-G-A

181145489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50280255-G-A

181145489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50280255-G-T

181145573-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50280171-G-C

181145659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50280085-A-G

181145715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50280029-C-T

181146679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50279111-A-G

181146863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50278937-T-C

181146983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50278822-C-T

181147174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50278672-C-T

181148027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50277798-T-C

181148110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50277716-C-T

181148111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50277715-G-A

181148225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50277602-G-A

181148310-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50277515-T-A

181148310-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50277515-T-G

181148574-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50277354-C-G

181148731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50277205-G-A

181148889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50277063-A-G

181148953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50276999-C-T

181149103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50276839-A-G

181149441-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50276483-T-A

181149441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50276483-T-C

181149509-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50276431-T-A

181149509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50276431-T-C

181149510-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50276430-A-T

http://identifiers.org/hco/4/GRCh38#181149511-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#50276429-A-C

http://identifiers.org/hco/4/GRCh38#181150043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#50276304-C-A

181150090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50276257-C-T

181150653-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50275696-A-T

181150779-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50275517-G-C

181150875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50275421-G-A

181150921-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50275372-T-A

181150928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50275365-T-C

181150960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50275269-A-G

181150970-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50275263-C-G

181150970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50275263-C-T

181151266-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50274936-A-T

181151327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50274855-A-G

181151369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50274782-A-G

181151370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50274781-A-G

181151370-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50274781-A-T

181151387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50274760-T-C

181151455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50274721-G-A

181151455-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50274721-G-C

181151455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50274721-G-T

181151613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50274579-C-T

181151638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50274549-T-C

181151709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50274482-T-C

181151732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50274459-G-A

181152032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50274204-G-A

181152039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50274197-G-A

181152136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50274098-G-A

181152175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50274059-T-C

181152222-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50274014-T-G

181152229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50274008-T-C

181152233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50274004-C-G

181152233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50274004-C-T

181152249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50273989-A-G

181153106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50273929-A-G

181153691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50273480-C-T

181155244-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50266796-C-G

181155340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50266685-C-T

181155353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50266672-G-T

181155560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50266480-G-T

181155647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: non coding transcript exon variant
orthologous variants: 50266393-G-A

181155680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: non coding transcript exon variant
orthologous variants: 50266359-T-C

181155680-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: non coding transcript exon variant
orthologous variants: 50266359-T-G

181155715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: non coding transcript exon variant
orthologous variants: 50266324-G-A

181155715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: non coding transcript exon variant
orthologous variants: 50266324-G-T

181155837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50266153-G-A

181155837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50266153-G-T

181155877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50266058-T-C

181155916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50266019-G-A

181156298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50265682-G-A

181156925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50265374-G-T

181158025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50264581-A-G

181158145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50264452-T-C

181158240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50263641-A-G

181158315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50263570-T-C

http://identifiers.org/hco/4/GRCh38#181158399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#50263489-C-A

181158682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50263204-T-C

181158849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50263041-A-G

181159045-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50262839-C-G

181159045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50262839-C-T

http://identifiers.org/hco/4/GRCh38#181159070-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#50262812-A-C

181159142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38515
most severe consequence: non coding transcript exon variant
orthologous variants: 50262740-C-T