143790930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75919017-T-C

143790930-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75919017-T-G

http://identifiers.org/hco/8/GRCh38#143791223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75919301-C-A

143791223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75919301-C-T

143791313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 75919392-A-G

http://identifiers.org/hco/8/GRCh38#143791345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75919419-C-A

143791345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75919419-C-T

143791603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75919703-G-A

143791603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75919703-G-T

143791909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 75919997-G-A

143791909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 75919997-G-T

143792076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75920156-C-T

http://identifiers.org/hco/8/GRCh38#143792167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75920257-C-A

143792167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75920257-C-T

143792291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75920362-G-A

143792291-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75920362-G-C

143792291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75920362-G-T

143792404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, stop_gained
orthologous variants: 75920475-G-A

143792404-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 75920475-G-C

143792404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 75920475-G-T

143792600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75920671-G-A

143792600-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75920671-G-C

143792600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75920671-G-T

http://identifiers.org/hco/8/GRCh38#143792718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75920793-C-A

143792718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75920793-C-T

143792751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75920826-G-A

143792751-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75920826-G-C

143792751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75920826-G-T

143792757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75920832-G-A

143792757-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75920832-G-C

143792757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75920832-G-T

http://identifiers.org/hco/8/GRCh38#143792991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75921067-C-A

143792991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75921067-C-T

http://identifiers.org/hco/8/GRCh38#143793059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/15/GRCm39#75921135-C-A

http://identifiers.org/hco/8/GRCh38#143793174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75921222-C-A

143793174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75921222-C-T

143793186-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75921234-T-A

143793186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75921234-T-C

143793214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75921261-G-A

143793214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75921261-G-T

143793408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75921464-G-A

143793408-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75921464-G-C

143793408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75921464-G-T

143793537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75921638-G-A

143793537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75921638-G-T

143793547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75921648-G-A

143793547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75921648-G-T

143793552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75921661-G-A

143793552-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75921661-G-C

143793552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75921661-G-T

http://identifiers.org/hco/8/GRCh38#143793591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75921686-C-A

143793591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75921686-C-T

http://identifiers.org/hco/8/GRCh38#143793639-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75921729-A-C

143793639-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75921729-A-T

http://identifiers.org/hco/8/GRCh38#143793748-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75921815-A-C

143793748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75921815-A-G

143793748-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75921815-A-T

143793932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75921931-C-T

143793934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75921933-A-G

http://identifiers.org/hco/8/GRCh38#143793945-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75921944-A-C

143793968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 75921967-G-A

143794137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75922147-G-A

143794137-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75922147-G-C

143794137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75922147-G-T

http://identifiers.org/hco/8/GRCh38#143794181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75922212-C-A

143794181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75922212-C-T

143794215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75922262-G-A

143794215-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75922262-G-C

143794215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75922262-G-T

143794242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75922290-A-G

143794243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75922291-G-A

143794243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75922291-G-T

http://identifiers.org/hco/8/GRCh38#143794248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75922296-C-A

143794248-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75922296-C-G

143794248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75922296-C-T

143794658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75922663-C-T

143794723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75922760-C-T

143794754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, undefined
orthologous variants: 75922843-C-T

http://identifiers.org/hco/8/GRCh38#143794910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75923059-C-A

143794910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75923059-C-T

http://identifiers.org/hco/8/GRCh38#143794951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75923133-C-A

143794951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75923133-C-T

143794953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75923135-C-T

143794969-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75923165-T-G

143795020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75923225-T-C

143795020-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75923225-T-G

143795029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75923235-G-A

143795029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75923235-G-T

143795257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75923456-G-A

143795257-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75923456-G-C

143795297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: missense variant
orthologous variants: 75923490-G-A

143795298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: synonymous variant
orthologous variants: 75923491-C-T

143795570-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75923752-C-G

http://identifiers.org/hco/8/GRCh38#143795632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75923790-C-A

143795632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75923790-C-T

http://identifiers.org/hco/8/GRCh38#143795645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75923803-C-A

143795789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75923931-G-A

143795789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75923931-G-T

143795962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75924092-G-A

143796114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75924212-G-A

143796321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75924387-G-A

143796475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75924494-G-A

143796659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75924667-C-T

143796722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75924730-G-C

143796800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75924808-G-T

143797068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75925104-G-A

143802194-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75928259-G-C

143802304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75928398-G-A

143802426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75928521-C-T

143802444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75928526-G-A

143802719-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75928693-T-A

143802719-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75928693-T-G

143802777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75928777-G-A

http://identifiers.org/hco/8/GRCh38#143803060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75929019-C-A

143803060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75929019-C-T

143803166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75929109-G-A

http://identifiers.org/hco/8/GRCh38#143803232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75929152-C-A

http://identifiers.org/hco/8/GRCh38#143803244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75929156-C-A

143803244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75929156-C-T

http://identifiers.org/hco/8/GRCh38#143803250-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75929162-A-C

143803250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75929162-A-G

143803250-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75929162-A-T

143803361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75929215-T-C

143803404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: synonymous variant
orthologous variants: 75929257-G-A

143803404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: synonymous variant
orthologous variants: 75929257-G-T

http://identifiers.org/hco/8/GRCh38#143803446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75929299-C-A

143803446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: synonymous variant
orthologous variants: 75929299-C-T

143803490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: synonymous variant
orthologous variants: 75929343-G-A

143803490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: missense variant
orthologous variants: 75929343-G-T

http://identifiers.org/hco/8/GRCh38#143803694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75929541-C-A

143803694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: missense variant
orthologous variants: 75929541-C-T

143803746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: synonymous variant
orthologous variants: 75929593-C-T

143803806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: synonymous variant
orthologous variants: 75929653-C-T

http://identifiers.org/hco/8/GRCh38#143803884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75929731-C-A

143803973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75929806-A-G

http://identifiers.org/hco/8/GRCh38#143803977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75929810-C-A

143803977-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75929810-C-G

143803977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75929810-C-T

143804032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75929861-A-G

143804032-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75929861-A-T

143804126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: synonymous variant
orthologous variants: 75929955-G-A

143804126-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: missense variant
orthologous variants: 75929955-G-C

143804201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75930019-G-A

143804288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75930103-G-A

143804288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75930103-G-T

143804325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75930136-C-T

143804334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75930145-A-G

143804439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75930635-A-G

143804439-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75930635-A-T

143804526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75930758-G-A

143804526-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75930758-G-C

143804526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75930758-G-T

143804532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75930782-G-A

143804532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75930782-G-T

143804543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75930792-G-A

143804543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75930792-G-T

http://identifiers.org/hco/8/GRCh38#143804565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75930808-C-A

143804565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75930808-C-T

http://identifiers.org/hco/8/GRCh38#143804639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75930882-C-A

143804639-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: missense variant
orthologous variants: 75930882-C-G

143804639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: missense variant
orthologous variants: 75930882-C-T

http://identifiers.org/hco/8/GRCh38#143804675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75930918-C-A

143804675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: missense variant
orthologous variants: 75930918-C-T

143804677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: missense variant
orthologous variants: 75930920-G-A

http://identifiers.org/hco/8/GRCh38#143804694-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75930937-A-C

143804694-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: missense variant
orthologous variants: 75930937-A-T

143804706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: synonymous variant
orthologous variants: 75930949-G-A

143804706-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: missense variant
orthologous variants: 75930949-G-C

143804799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: synonymous variant
orthologous variants: 75931042-G-A

143804799-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: synonymous variant
orthologous variants: 75931042-G-C

143804799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: synonymous variant
orthologous variants: 75931042-G-T

143804828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 75931071-G-A

143804828-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 75931071-G-C

143804828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 75931071-G-T

143804859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75931094-G-A

143804859-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75931094-G-C

143804859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75931094-G-T

143804889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75931126-G-A

143804890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75931127-G-A

143804890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75931127-G-T

http://identifiers.org/hco/8/GRCh38#143804922-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75931135-A-C

http://identifiers.org/hco/8/GRCh38#143804955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75931168-C-A

143804955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 75931168-C-G

143804955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 75931168-C-T

143804997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: synonymous variant
orthologous variants: 75931210-G-A

143804997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: synonymous variant
orthologous variants: 75931210-G-T

143805040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75931259-G-T

143805078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75931295-A-G

143805139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: synonymous variant
orthologous variants: 75931359-G-A

143805139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: synonymous variant
orthologous variants: 75931359-G-T

143805216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: missense variant
orthologous variants: 75931436-G-A

143805216-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: missense variant
orthologous variants: 75931436-G-C

143805216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: missense variant
orthologous variants: 75931436-G-T

143805256-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: synonymous variant
orthologous variants: 75931476-C-G

143805256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: synonymous variant
orthologous variants: 75931476-C-T

143805412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: synonymous variant
orthologous variants: 75931632-G-A

143805412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: synonymous variant
orthologous variants: 75931632-G-T

143805448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75931668-G-A

143805448-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75931668-G-C

143805448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75931668-G-T

143805962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75932014-C-T

143806052-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75932084-T-A

143806052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75932084-T-C

143806077-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75932112-A-T

143806258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75932263-G-A

143806258-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75932263-G-C

http://identifiers.org/hco/8/GRCh38#143806271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75932287-C-A

143806271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75932287-C-T

http://identifiers.org/hco/8/GRCh38#143806274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75932290-C-A

143806274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75932290-C-T

http://identifiers.org/hco/8/GRCh38#143806316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75932325-C-A

143806316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75932325-C-T

http://identifiers.org/hco/8/GRCh38#143806330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75932335-C-A

143806330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75932335-C-T

143806344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75932349-C-G

143806344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75932349-C-T

143806354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75932361-T-C

143806354-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75932361-T-G

143806372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75932378-A-G

143806372-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75932378-A-T

143806452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: synonymous variant
orthologous variants: 75932461-G-A

143806452-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: synonymous variant
orthologous variants: 75932461-G-C

143806452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: synonymous variant
orthologous variants: 75932461-G-T

143806547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75932569-G-A

143806547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75932569-G-T

143806679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75932700-C-G

143806773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75932804-T-C

143807037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75933098-T-C

http://identifiers.org/hco/8/GRCh38#143807038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75933099-C-A

143807038-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75933099-C-G

143807038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75933099-C-T

143807127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75933200-G-A

143807127-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75933200-G-C

143807127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75933200-G-T

143807350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75933351-T-C

143807358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75933359-C-T

143807423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75933439-G-A

143807423-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75933439-G-C

143807423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75933439-G-T

http://identifiers.org/hco/8/GRCh38#143807483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75933509-C-A

143807483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75933509-C-T

http://identifiers.org/hco/8/GRCh38#143807714-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75933748-A-C

143807714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75933748-A-G

143807738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75933768-C-T

143807741-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75933771-G-C

143807741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75933771-G-T

143808059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75934083-G-A

143808111-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75934150-G-C

143808594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75934506-G-A

143808594-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75934506-G-C

143808596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75934508-G-A

http://identifiers.org/hco/8/GRCh38#143808690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75934603-C-A

143808690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: synonymous variant
orthologous variants: 75934603-C-T

http://identifiers.org/hco/8/GRCh38#143808696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75934609-C-A

143808696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: synonymous variant
orthologous variants: 75934609-C-T

143808822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: synonymous variant
orthologous variants: 75934693-A-G

143808966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: synonymous variant
orthologous variants: 75934837-C-T

143809101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75934964-G-A

143809101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75934964-G-T

143809160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75935012-G-T

143809235-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75935083-T-A

143809290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75935143-G-A

143809290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75935143-G-T

http://identifiers.org/hco/8/GRCh38#143809399-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75935269-A-C

143809399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75935269-A-G

143809399-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75935269-A-T

143809440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75935310-G-A

143809440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75935310-G-T

143809450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75935320-G-A

143809450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75935320-G-T

143809451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75935321-G-A

143809451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75935321-G-T

143809477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75935356-A-G

143809477-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75935356-A-T

143809554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: synonymous variant
orthologous variants: 75935443-C-T

http://identifiers.org/hco/8/GRCh38#143809653-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75935539-A-C

143809653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: synonymous variant
orthologous variants: 75935539-A-G

143809766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75935652-G-A

143809766-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75935652-G-C

143809766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75935652-G-T

http://identifiers.org/hco/8/GRCh38#143809824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75935693-C-A

143809824-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75935693-C-G

143809824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75935693-C-T

143810047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75935904-C-T

143810155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75936010-C-T

143810222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75936082-G-A

http://identifiers.org/hco/8/GRCh38#143810288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75936150-C-A

143810382-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75936251-T-A

143810416-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75936286-T-A

143810416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75936286-T-C

143810428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75936297-C-T

143810464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75936313-T-C

143810698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: synonymous variant
orthologous variants: 75936558-T-C

143810830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75936689-G-A

http://identifiers.org/hco/8/GRCh38#143810831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75936690-C-A

143810831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75936690-C-T

143810835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75936694-A-G

143810847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75936707-A-G

143810887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75936739-C-T

143810958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: synonymous variant
orthologous variants: 75936811-G-A

143810958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: synonymous variant
orthologous variants: 75936811-G-T

143811003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: synonymous variant
orthologous variants: 75936856-C-T

143811181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: synonymous variant
orthologous variants: 75937034-C-T

143811184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: synonymous variant
orthologous variants: 75937037-G-A

143811526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75937383-C-T

143811549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75937406-G-A

143811564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75937415-T-C

143811632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75937477-C-T

143811689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75937511-G-A

143811887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75937661-G-A

143811888-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75937662-G-C

143811889-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75937663-T-G

143811955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75937717-T-C

143812212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75937893-T-C

143812213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75937894-T-C

http://identifiers.org/hco/8/GRCh38#143812226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75937909-C-A

143812226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75937909-C-T

143812235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75937918-C-T

143812245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75937928-G-A

143812245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75937928-G-T

143812418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75938112-C-T

http://identifiers.org/hco/8/GRCh38#143812462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75938148-C-A

143812462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75938148-C-T

http://identifiers.org/hco/8/GRCh38#143812464-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75938150-A-C

143812464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75938150-A-G

http://identifiers.org/hco/8/GRCh38#143812481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75938178-C-A

143812481-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75938178-C-G

143812481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75938178-C-T

143812503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75938200-G-A

143812503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75938200-G-T

143812514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75938205-G-A

143812514-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75938205-G-C

143812514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75938205-G-T

http://identifiers.org/hco/8/GRCh38#143812568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75938256-C-A

http://identifiers.org/hco/8/GRCh38#143812669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75938359-C-A

143812669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75938359-C-T

143812687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75938375-A-G

143812818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 75938460-G-A

http://identifiers.org/hco/8/GRCh38#143812866-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75938508-A-C

143812866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: synonymous variant
orthologous variants: 75938508-A-G

http://identifiers.org/hco/8/GRCh38#143813146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75938773-C-A

143813146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75938773-C-T

http://identifiers.org/hco/8/GRCh38#143813185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75938781-C-A

143813185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75938781-C-T

143813262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75938817-G-A

143813390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75938922-G-A

143813390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75938922-G-T

143813427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75938956-G-A

143813508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: synonymous variant
orthologous variants: 75939032-G-A

143813508-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: synonymous variant
orthologous variants: 75939032-G-C

http://identifiers.org/hco/8/GRCh38#143813567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75939084-C-A

143813567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75939084-C-T

143813612-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75939112-T-A

143813612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75939112-T-C

143813695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: synonymous variant
orthologous variants: 75939197-G-A

143813915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75939425-G-A

http://identifiers.org/hco/8/GRCh38#143813956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75939464-C-A

143813956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75939464-C-T

143813966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75939472-C-T

143813985-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75939494-T-A

143813985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75939494-T-C

143813985-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75939494-T-G

http://identifiers.org/hco/8/GRCh38#143813990-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75939499-A-C

143813990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75939499-A-G

143813994-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 75939503-T-A

143813994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 75939503-T-C

143813994-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 75939503-T-G

143814014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: synonymous variant
orthologous variants: 75939523-G-A

143814014-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: missense variant
orthologous variants: 75939523-G-C

143814014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: missense variant
orthologous variants: 75939523-G-T

143814248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75939764-G-A

143814248-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75939764-G-C

143814248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75939764-G-T

143814250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75939766-G-A

143814250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75939766-G-T

http://identifiers.org/hco/8/GRCh38#143814704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75940505-C-A

143814704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75940505-C-T

143814728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, undefined
orthologous variants: 75940528-G-A

143814728-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, undefined
orthologous variants: 75940528-G-C

143814728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, undefined
orthologous variants: 75940528-G-T

143814753-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, undefined
orthologous variants: 75940577-C-G

143814753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron_variant, undefined
orthologous variants: 75940577-C-T

143814803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75940642-G-A

143814803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75940642-G-T

143814866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 75940724-A-G

http://identifiers.org/hco/8/GRCh38#143814880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75940738-C-A

143814880-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 75940738-C-G

143814880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 75940738-C-T

http://identifiers.org/hco/8/GRCh38#143814913-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#75940770-A-C

http://identifiers.org/hco/8/GRCh38#143814917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#75940774-C-A

143815110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75940949-G-A

143815110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75940949-G-C

143815110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75940949-G-T

143815138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75940977-C-G

143815138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: intron variant
orthologous variants: 75940977-C-T

143815554-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: 5 prime UTR variant
orthologous variants: 75941427-C-G

143815565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30377
most severe consequence: 5 prime UTR variant
orthologous variants: 75941438-C-T