81395822-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120124107-A-T

81395823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120124108-A-G

81395852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120124145-C-T

81396006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120124298-G-T

http://identifiers.org/hco/17/GRCh38#81396015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120124307-C-A

81396015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120124307-C-T

81396432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120124700-G-A

81396432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120124700-G-T

81396618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120124890-G-T

81396725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120124996-G-A

81396725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120124996-G-T

81396752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120125013-A-G

81396785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120125046-G-T

81396788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120125049-A-G

81396898-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120125140-T-A

81396898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120125140-T-C

81396898-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120125140-T-G

81397017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120125239-C-T

http://identifiers.org/hco/17/GRCh38#81397113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120125321-C-A

81397113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120125321-C-T

http://identifiers.org/hco/17/GRCh38#81397217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120125421-C-A

81397217-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120125421-C-G

81397217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120125421-C-T

81397258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120125461-G-A

81397258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120125461-G-T

81397260-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120125463-T-A

http://identifiers.org/hco/17/GRCh38#81397273-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120125476-A-C

81397273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120125476-A-G

http://identifiers.org/hco/17/GRCh38#81397275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120125478-C-A

81397275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120125478-C-T

81397321-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120125523-T-G

81397436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120125626-A-G

81398292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120126450-C-T

81398361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120126518-G-A

81399039-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120127186-T-G

http://identifiers.org/hco/17/GRCh38#81399258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120127406-C-A

81399258-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 120127406-C-G

81399258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 120127406-C-T

81399928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120128094-G-A

81399928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120128094-G-T

http://identifiers.org/hco/17/GRCh38#81399980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120128164-C-A

81399980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120128164-C-T

http://identifiers.org/hco/17/GRCh38#81399981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120128165-C-A

81399981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120128165-C-T

http://identifiers.org/hco/17/GRCh38#81399997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120128181-C-A

81399997-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120128181-C-G

81399997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120128181-C-T

81400080-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120128236-C-G

81400711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120128807-G-A

81400711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120128807-G-T

http://identifiers.org/hco/17/GRCh38#81401005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120129033-C-A

http://identifiers.org/hco/17/GRCh38#81401173-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120129200-A-C

81401245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120129275-G-A

81401245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120129275-G-T

http://identifiers.org/hco/17/GRCh38#81401273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120129300-C-A

81401273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120129300-C-T

81401360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120129391-T-C

81401494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120129535-G-A

81401494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120129535-G-T

http://identifiers.org/hco/17/GRCh38#81401529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120129565-C-A

81401529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120129565-C-T

http://identifiers.org/hco/17/GRCh38#81401711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#120129771-C-A

81401790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120129835-A-G

81401835-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120129887-A-T

81401858-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120129915-T-A

http://identifiers.org/hco/17/GRCh38#81401880-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120129938-A-C

81402135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120130160-G-A

http://identifiers.org/hco/17/GRCh38#81402198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#120130223-C-A

81402198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120130223-C-G

81402198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120130223-C-T

81402463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120130455-A-G

81402463-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120130455-A-T

81402547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120130552-G-A

81402579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120130588-T-C

81402696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120130705-G-T

81402738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120130726-G-A

81402741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120130729-G-A

81402741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120130729-G-T

http://identifiers.org/hco/17/GRCh38#81402797-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120130776-A-C

http://identifiers.org/hco/17/GRCh38#81402798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120130777-C-A

81402798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120130777-C-T

81402901-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120130909-C-G

81402901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120130909-C-T

81403096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120131127-T-C

81403107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120131138-G-A

81403107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120131138-G-T

81403115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120131148-T-C

81403115-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120131148-T-G

81403192-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120131230-C-G

http://identifiers.org/hco/17/GRCh38#81403531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120131530-C-A

81403754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120131780-A-G

http://identifiers.org/hco/17/GRCh38#81403852-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120131886-A-C

http://identifiers.org/hco/17/GRCh38#81404164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120132199-C-A

81404459-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120132501-G-C

81404465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120132507-G-A

81404472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120132514-G-A

81404570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120132600-T-C

81404583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120132612-C-T

81404590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120132619-G-A

81404894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120132912-T-C

81405004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120133014-T-C

81405443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120133084-G-A

81405598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120133222-T-C

81405598-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120133222-T-G

81406248-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120133764-G-C

81406325-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120133866-G-C

81406698-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120134241-C-G

http://identifiers.org/hco/17/GRCh38#81406782-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120134309-A-C

81406782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120134309-A-G

81406800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120134327-G-C

81406800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120134327-G-T

81406837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120134363-G-A

81407010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120134531-C-T

81407197-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120134702-T-G

http://identifiers.org/hco/17/GRCh38#81407221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120134743-C-A

81407221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120134743-C-T

81407229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120134752-A-G

81407232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120134755-G-A

81407297-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120134819-G-C

81407338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120134854-A-G

81407376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120134922-C-T

81407753-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120135351-T-G

81407970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120135595-C-T

81408127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120135718-G-A

81408127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120135718-G-T

81408368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120135967-C-T

81408489-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120136096-G-C

81412547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120136559-C-T

81412553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120136572-C-T

81412717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120136755-C-T

81413055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120137060-C-T

81413078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120137077-A-G

http://identifiers.org/hco/17/GRCh38#81413114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120137118-C-A

81413114-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120137118-C-G

81413114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120137118-C-T

81413134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120137138-G-A

http://identifiers.org/hco/17/GRCh38#81413150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120137154-C-A

81413150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120137154-C-T

http://identifiers.org/hco/17/GRCh38#81413177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120137164-C-A

81413177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120137164-C-T

81413189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120137176-T-C

http://identifiers.org/hco/17/GRCh38#81413217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120137191-C-A

81413217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120137191-C-T

http://identifiers.org/hco/17/GRCh38#81413218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120137192-C-A

81413218-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120137192-C-G

81413218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120137192-C-T

81413229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120137203-T-C

http://identifiers.org/hco/17/GRCh38#81413295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120137233-C-A

81413295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120137233-C-T

81413347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120137275-G-A

81413557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120137497-G-A

81413667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120137590-G-A

81413721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120137627-A-G

81414081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120138052-G-A

81414081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120138052-G-T

81415335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120139637-G-A

http://identifiers.org/hco/17/GRCh38#81415403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120139679-C-A

81415421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120139703-G-A

81415421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120139703-G-C

81415421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120139703-G-T

http://identifiers.org/hco/17/GRCh38#81415422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120139704-C-A

81415422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120139704-C-T

81415471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120139750-G-A

81415471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120139750-G-T

81415480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120139759-G-A

81415480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120139759-G-T

81415526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120139805-T-C

81415624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120139908-G-A

81415624-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120139908-G-C

81415624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120139908-G-T

http://identifiers.org/hco/17/GRCh38#81415700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120139972-C-A

81415700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120139972-C-T

81415771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120140040-C-G

81416711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120141220-G-A

81416716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120141225-C-T

81416826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120141320-C-T

81416876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120141372-T-C

81417140-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120141674-G-C

81417340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120141934-C-T

81417341-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120141935-T-G

81417355-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120141949-G-C

81417389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120141985-A-G

81417459-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120142041-C-G

81417459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120142041-C-T

81418718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120143124-G-A

81418941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120143336-C-T

81419367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120143709-G-A

81419368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120143710-C-T

81419380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120143722-C-T

81419435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, undefined
orthologous variants: 120143775-C-T

81419485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, undefined
orthologous variants: 120143816-T-C

81419733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120144100-G-A

81420831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120145700-C-T

81421162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120145929-C-T

81421463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120146246-C-T

http://identifiers.org/hco/17/GRCh38#81422736-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120147292-A-C

81422736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120147292-A-G

81422854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120147389-G-A

81422854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120147389-G-T

81422884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120147428-G-A

81422884-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120147428-G-C

81422884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120147428-G-T

81422923-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120147459-C-G

81422923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120147459-C-T

81422960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120147504-C-T

81423700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120148143-C-T

81423737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120148167-T-C

81423971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120148400-C-T

81424290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120148697-G-T

81424333-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120148734-C-G

81424388-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120148811-C-G

81424592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 25492912-G-A

81424736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: -G-T

81424739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 25492755-A-G

81424832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 25492655-G-A

81424869-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 25492620-G-C

81424872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 25492617-G-T

81424948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 25492529-G-A

81424948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 25492529-G-T

81424970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 25493073-G-A

81424970-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 25493073-G-C

81424970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 25493073-G-T

81425017-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 25493022-T-G

81425042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 25492993-G-A

81425042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 25492993-G-T

81425044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 25492991-T-C

81425044-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 25492991-T-G

81425052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 25492983-G-A

81425052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 25492983-G-T

81425065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 25492969-A-G

81425065-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 25492969-A-T

81425106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 25492927-G-A

81425890-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120149081-T-A

81425928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, undefined
orthologous variants: 120149119-A-G

81425928-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, undefined
orthologous variants: 120149119-A-T

81425936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, undefined
orthologous variants: 120149127-A-G

81425936-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, undefined
orthologous variants: 120149127-A-T

81426026-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120149191-T-A

81426026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120149191-T-C

81426051-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120149210-T-G

81426126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120149277-A-G

81426126-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120149277-A-T

81426143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120149280-G-A

81426143-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120149280-G-C

81426161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120149300-G-A

81426176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120149315-G-T

81426182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120149321-T-C

81426182-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120149321-T-G

81426331-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120149436-G-C

81426389-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120149497-T-G

81426399-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120149510-C-G

81426399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120149510-C-T

81426401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120149512-T-C

81426401-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120149512-T-G

81426456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120149581-G-T

81426556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120149667-A-G

http://identifiers.org/hco/17/GRCh38#81426741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120149842-C-A

81426777-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120149875-T-A

81426777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120149875-T-C

http://identifiers.org/hco/17/GRCh38#81426840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120149938-C-A

81426840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense variant
orthologous variants: 120149938-C-G

81426844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense variant
orthologous variants: 120149942-G-A

81426844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense variant
orthologous variants: 120149942-G-T

http://identifiers.org/hco/17/GRCh38#81426879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120149977-C-A

http://identifiers.org/hco/17/GRCh38#81426963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120150061-C-A

81426963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: synonymous variant
orthologous variants: 120150061-C-T

81427425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120150443-G-T

81427640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120150665-G-A

81428528-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120151531-T-G

81428654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120151644-C-T

81428882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120151857-T-C

81428895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120151868-A-G

81429708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, undefined
orthologous variants: 120152657-C-T

81430201-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120153181-G-C

81430201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120153181-G-T

81435863-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120155871-C-G

81435871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120155882-G-A

81436247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120156144-C-T

81436729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120156570-C-T

81437770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120158543-A-G

81437899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120158655-C-T

81438176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120158942-G-A

81438276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120159041-G-A

81438276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120159041-G-T

81438289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120159054-T-C

81438294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120159059-G-A

81438294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120159059-G-T

http://identifiers.org/hco/17/GRCh38#81438314-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120159078-A-C

81438314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120159078-A-G

81438367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 120159130-T-C

http://identifiers.org/hco/17/GRCh38#81438500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120159263-C-A

81438502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120159265-G-A

81438502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120159265-G-T

http://identifiers.org/hco/17/GRCh38#81438504-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120159266-A-C

81438504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120159266-A-G

81438564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120159311-G-T

81438567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120159314-A-G

81438567-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120159314-A-T

81438620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120159335-G-T

http://identifiers.org/hco/17/GRCh38#81439398-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120159835-A-C

81439427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120159869-C-T

81439436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120159877-G-A

81439444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120159885-G-A

81439448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120159889-C-T

81439485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120159899-T-C

81439501-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120159907-T-G

81439548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120159939-T-C

81439548-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120159939-T-G

81439687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120160040-C-T

81439779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120160148-C-T

81440293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120160587-G-A

81440705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120160998-G-A

81441070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, undefined
orthologous variants: 120161440-C-T

81441072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, undefined
orthologous variants: 120161442-C-T

81441684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120162091-A-G

81441684-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120162091-A-T

81441768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120162117-A-G

81441768-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120162117-A-T

http://identifiers.org/hco/17/GRCh38#81441895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120162249-C-A

81442108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: synonymous variant
orthologous variants: 120162456-G-A

81442108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: synonymous variant
orthologous variants: 120162456-G-T

81442170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense variant
orthologous variants: 120162518-A-G

http://identifiers.org/hco/17/GRCh38#81442195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120162543-C-A

81442238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense variant
orthologous variants: 120162586-G-A

81442238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense variant
orthologous variants: 120162586-G-T

81442279-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: synonymous variant
orthologous variants: 120162627-T-A

81442279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: synonymous variant
orthologous variants: 120162627-T-C

81442294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: synonymous variant
orthologous variants: 120162642-G-A

81442294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: synonymous variant
orthologous variants: 120162642-G-T

http://identifiers.org/hco/17/GRCh38#81442448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120162820-C-A

81442448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: synonymous variant
orthologous variants: 120162820-C-T

http://identifiers.org/hco/17/GRCh38#81442687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120163059-C-A

81442687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: synonymous variant
orthologous variants: 120163059-C-T

81442777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: synonymous variant
orthologous variants: 120163146-C-T

81442928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense variant
orthologous variants: 120163294-G-A

81443003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense variant
orthologous variants: 120163369-G-A

81443056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: synonymous variant
orthologous variants: 120163422-G-A

81443341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: synonymous variant
orthologous variants: 120163707-G-A

81443341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense variant
orthologous variants: 120163707-G-T

81443393-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense variant
orthologous variants: 120163759-G-C

81443393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense variant
orthologous variants: 120163759-G-T

81443437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: synonymous variant
orthologous variants: 120163803-G-T

http://identifiers.org/hco/17/GRCh38#81443595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120163959-C-A

81443595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120163959-C-T

81443691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120164036-A-G

81443694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120164039-G-A

81443694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120164039-G-T

81443697-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120164042-T-A

81443754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120164086-G-T

http://identifiers.org/hco/17/GRCh38#81443776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120164109-C-A

81443822-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120164154-C-G

http://identifiers.org/hco/17/GRCh38#81443836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120164168-C-A

81443836-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120164168-C-G

81443836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120164168-C-T

81443837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120164169-G-A

81443837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120164169-G-T

http://identifiers.org/hco/17/GRCh38#81443900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120164232-C-A

81443900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120164232-C-T

81443909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120164241-G-A

81443909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120164241-G-T

81443967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120164277-G-T

81443968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120164278-G-A

81443968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120164278-G-T

81443969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120164279-G-A

81443969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120164279-G-T

81444095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120164380-G-A

81444095-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120164380-G-C

http://identifiers.org/hco/17/GRCh38#81444489-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120164616-A-C

81444489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: synonymous variant
orthologous variants: 120164616-A-G

http://identifiers.org/hco/17/GRCh38#81444507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120164637-C-A

81444507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: synonymous variant
orthologous variants: 120164637-C-T

81444510-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense variant
orthologous variants: 120164640-T-A

81444510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: synonymous variant
orthologous variants: 120164640-T-C

81444534-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: synonymous variant
orthologous variants: 120164664-C-G

81444534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: synonymous variant
orthologous variants: 120164664-C-T

81444571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120164701-C-T

81444839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120164981-G-A

81444839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120164981-G-T

81444947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120165170-G-A

81444947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120165170-G-T

http://identifiers.org/hco/17/GRCh38#81444992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120165222-C-A

81444992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120165222-C-T

http://identifiers.org/hco/17/GRCh38#81445208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120165560-C-A

81445208-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120165560-C-G

81445208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120165560-C-T

http://identifiers.org/hco/17/GRCh38#81445226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120165578-C-A

81445226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120165578-C-T

81445272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120165627-T-C

http://identifiers.org/hco/17/GRCh38#81445292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120165647-C-A

http://identifiers.org/hco/17/GRCh38#81445513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120165860-C-A

81445513-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense variant
orthologous variants: 120165860-C-G

81445513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense variant
orthologous variants: 120165860-C-T

http://identifiers.org/hco/17/GRCh38#81445714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120166065-C-A

81445714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120166065-C-T

http://identifiers.org/hco/17/GRCh38#81445732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120166091-C-A

81445732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120166091-C-T

81445946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120166248-G-A

81446025-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120166323-C-G

81446297-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120166577-C-G

81446297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120166577-C-T

81446584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120166774-T-C

81447244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: synonymous variant
orthologous variants: 120167089-G-A

81447481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: synonymous variant
orthologous variants: 120167329-G-A

81447522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense variant
orthologous variants: 120167367-G-T

http://identifiers.org/hco/17/GRCh38#81447610-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120167461-A-C

81447618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense variant
orthologous variants: 120167469-A-G

81447760-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: synonymous variant
orthologous variants: 120167611-T-A

81447760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: synonymous variant
orthologous variants: 120167611-T-C

http://identifiers.org/hco/17/GRCh38#81447872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120167723-C-A

http://identifiers.org/hco/17/GRCh38#81447876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120167727-C-A

81447876-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120167727-C-G

81447879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120167730-A-G

81447968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120167807-T-C

81448009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120167838-G-A

81448427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120168276-G-A

81448565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120168388-C-T

81448599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120168423-G-A

81448599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120168423-G-T

81449805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120169357-C-T

http://identifiers.org/hco/17/GRCh38#81451591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120169831-C-A

81451591-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120169831-C-G

81451591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120169831-C-T

81451619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120169847-G-T

http://identifiers.org/hco/17/GRCh38#81451664-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120169874-A-C

81451664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 120169874-A-G

81451672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: synonymous variant
orthologous variants: 120169882-G-A

http://identifiers.org/hco/17/GRCh38#81451715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120169925-C-A

http://identifiers.org/hco/17/GRCh38#81451783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120169993-C-A

81451783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: synonymous variant
orthologous variants: 120169993-C-T

http://identifiers.org/hco/17/GRCh38#81451807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120170017-C-A

81451807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: synonymous variant
orthologous variants: 120170017-C-T

81451909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120170137-T-C

81451910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120170138-G-A

81451910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120170138-G-T

81452182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120170400-G-A

81452182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120170400-G-T

81452546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120170739-G-A

http://identifiers.org/hco/17/GRCh38#81452600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120170781-C-A

81452600-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120170781-C-G

http://identifiers.org/hco/17/GRCh38#81452671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120170847-C-A

81452671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120170847-C-T

81452759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: synonymous variant
orthologous variants: 120170932-G-A

81452759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: synonymous variant
orthologous variants: 120170932-G-T

http://identifiers.org/hco/17/GRCh38#81452766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120170939-C-A

81452766-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense variant
orthologous variants: 120170939-C-G

81452766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense variant
orthologous variants: 120170939-C-T

http://identifiers.org/hco/17/GRCh38#81452858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120171031-C-A

81452858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 120171031-C-T

81452922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120171077-T-C

81452922-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120171077-T-G

81452929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120171084-T-C

81453768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120172118-G-A

81454228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120172624-G-A

81454228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120172624-G-C

81454228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120172624-G-T

81455115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120172809-C-T

81455428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120173097-C-T

81455433-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120173103-C-G

81455433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120173103-C-T

81456073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120173731-G-A

81456114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120173753-G-A

81456114-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120173753-G-C

81456114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120173753-G-T

81456195-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120173820-A-T

81456273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120173899-G-A

81456293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 120173918-A-G

81456299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 120173924-G-A

81456299-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 120173924-G-C

81456299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 120173924-G-T

http://identifiers.org/hco/17/GRCh38#81456306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120173931-C-A

81456306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 120173931-C-T

81456443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120174068-G-A

81456443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120174068-G-T

81456485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120174110-G-A

81456485-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120174110-G-C

81456485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120174110-G-T

81456486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120174111-G-A

81456486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120174111-G-T

http://identifiers.org/hco/17/GRCh38#81456497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120174122-C-A

81456497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120174122-C-T

81456503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120174128-G-A

81456503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120174128-G-T

http://identifiers.org/hco/17/GRCh38#81456504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120174129-C-A

81456504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120174129-C-T

81456580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120174205-A-G

81456613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120174231-C-T

81456849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120174416-C-T

81456909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120174478-C-T

http://identifiers.org/hco/17/GRCh38#81457111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120174646-C-A

81457179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120174691-G-A

81457179-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120174691-G-C

http://identifiers.org/hco/17/GRCh38#81457317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120174754-C-A

81457317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120174754-C-T

http://identifiers.org/hco/17/GRCh38#81457589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120174997-C-A

81457589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120174997-C-T

81457615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120175035-G-A

81457615-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120175035-G-C

81457615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120175035-G-T

81458138-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120175054-T-G

81458145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120175061-G-A

81458145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120175061-G-T

81458196-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120175111-G-C

81458196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120175111-G-T

81458322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120175237-G-A

81458322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120175237-G-C

81458322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120175237-G-T

http://identifiers.org/hco/17/GRCh38#81458338-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120175253-A-C

81458338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120175253-A-G

81458481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120175391-T-C

81458744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120175672-G-A

http://identifiers.org/hco/17/GRCh38#81458776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120175701-C-A

81458776-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120175701-C-G

81458776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120175701-C-T

81458798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120175718-T-C

81458798-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120175718-T-G

http://identifiers.org/hco/17/GRCh38#81458878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120175806-C-A

81458878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense variant
orthologous variants: 120175806-C-G

81458878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: synonymous variant
orthologous variants: 120175806-C-T

81458886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense variant
orthologous variants: 120175814-G-A

81458896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: synonymous variant
orthologous variants: 120175824-G-A

81458896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: synonymous variant
orthologous variants: 120175824-G-T

81458933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense variant
orthologous variants: 120175852-A-G

http://identifiers.org/hco/17/GRCh38#81459091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120176008-C-A

81459091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: synonymous variant
orthologous variants: 120176008-C-T

81459346-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120176275-C-G

81459346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120176275-C-T

81459406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120176334-C-T

81459480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120176378-G-A

81459582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120176483-G-A

81459655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120176558-G-A

81459693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120176589-G-A

81459693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120176589-G-T

81459700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120176595-G-T

http://identifiers.org/hco/17/GRCh38#81459701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120176596-C-A

81459701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120176596-C-T

http://identifiers.org/hco/17/GRCh38#81459745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120176641-C-A

81459785-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120176687-G-C

81459792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120176694-G-A

81459986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120176870-G-A

http://identifiers.org/hco/17/GRCh38#81459990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120176874-C-A

81459990-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120176874-C-G

81460033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120176919-C-T

81460258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120177105-T-C

http://identifiers.org/hco/17/GRCh38#81460267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120177116-C-A

81460267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120177116-C-T

81460311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120177158-A-G

http://identifiers.org/hco/17/GRCh38#81460462-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120177351-A-C

81460512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120177405-G-A

81460512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120177405-G-T

http://identifiers.org/hco/17/GRCh38#81460550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120177439-C-A

81460550-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120177439-C-G

81460629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120177518-G-A

81460629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120177518-G-T

81460648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120177537-G-A

81460648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120177537-G-T

81460666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120177555-G-T

81460720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120177608-C-T

http://identifiers.org/hco/17/GRCh38#81460806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120177688-C-A

81460806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120177688-C-T

81460987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120177871-G-A

81460987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120177871-G-T

http://identifiers.org/hco/17/GRCh38#81461089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120177988-C-A

81461089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120177988-C-T

http://identifiers.org/hco/17/GRCh38#81461122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120178021-C-A

81461122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120178021-C-T

81461256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 120178155-G-A

81461256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 120178155-G-T

http://identifiers.org/hco/17/GRCh38#81461344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120178243-C-A

81461344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 120178243-C-T

81461350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 120178249-G-A

81461350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 120178249-G-T

http://identifiers.org/hco/17/GRCh38#81461362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120178261-C-A

81461362-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 120178261-C-G

81461362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 120178261-C-T

81461391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 120178290-G-A

81461391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 120178290-G-T

81461401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 120178300-T-C

81461548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 120178429-G-A

81461548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 120178429-G-T

81461597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 120178478-G-A

81461597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 120178478-G-T

http://identifiers.org/hco/17/GRCh38#81461620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120178501-C-A

http://identifiers.org/hco/17/GRCh38#81461755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120178636-C-A

81461755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120178636-C-T

81462031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: synonymous variant
orthologous variants: 120178915-G-A

81462031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: synonymous variant
orthologous variants: 120178915-G-T

81462043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: synonymous variant
orthologous variants: 120178927-A-G

81462451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120179843-G-A

81462451-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120179843-G-C

81462451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120179843-G-T

81462460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120179852-A-G

81462481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120179873-A-G

81462481-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120179873-A-T

81462484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120179874-T-C

http://identifiers.org/hco/17/GRCh38#81462487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120179877-C-A

81462487-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120179877-C-G

81462487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120179877-C-T

81462542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120179934-G-A

81462542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron variant
orthologous variants: 120179934-G-T

81462565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120179960-A-G

http://identifiers.org/hco/17/GRCh38#81462702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120180089-C-A

81462702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120180089-C-T

81463542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120180433-T-C

81463561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120180450-G-T

http://identifiers.org/hco/17/GRCh38#81463577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120180466-C-A

81463577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120180466-C-T

81463619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120180511-G-A

81463619-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120180511-G-C

81463673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120180565-C-T

81464255-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: 3 prime UTR variant
orthologous variants: 120181089-G-C

81464255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: 3 prime UTR variant
orthologous variants: 120181089-G-T

http://identifiers.org/hco/17/GRCh38#81464291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120181154-C-A

81464291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: 3 prime UTR variant
orthologous variants: 120181154-C-T

81464295-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: 3 prime UTR variant
orthologous variants: 120181158-T-G

81464301-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: 3 prime UTR variant
orthologous variants: 120181164-T-G

81464303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: 3 prime UTR variant
orthologous variants: 120181166-T-C

http://identifiers.org/hco/17/GRCh38#81464305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120181168-C-A

81464305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: 3 prime UTR variant
orthologous variants: 120181168-C-T

http://identifiers.org/hco/17/GRCh38#81464307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120181170-C-A

81464307-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: 3 prime UTR variant
orthologous variants: 120181170-C-G

81464307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: 3 prime UTR variant
orthologous variants: 120181170-C-T

81464420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: 3 prime UTR variant
orthologous variants: 120181299-A-G

http://identifiers.org/hco/17/GRCh38#81464456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120181333-C-A

81464588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: 3 prime UTR variant
orthologous variants: 120181470-G-A

81464588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: 3 prime UTR variant
orthologous variants: 120181470-G-T

81464618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: 3 prime UTR variant
orthologous variants: 120181539-A-G

81464733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: 3 prime UTR variant
orthologous variants: 120181649-A-G

81464767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: 3 prime UTR variant
orthologous variants: 120181683-G-T

http://identifiers.org/hco/17/GRCh38#81464790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120181704-C-A

http://identifiers.org/hco/17/GRCh38#81464826-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120181740-A-C

81464826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: 3 prime UTR variant
orthologous variants: 120181740-A-G

81464826-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: 3 prime UTR variant
orthologous variants: 120181740-A-T

81464993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: 3 prime UTR variant
orthologous variants: 120181885-C-T

http://identifiers.org/hco/17/GRCh38#81465066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120181948-C-A

81465066-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: 3 prime UTR variant
orthologous variants: 120181948-C-G

81465066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: 3 prime UTR variant
orthologous variants: 120181948-C-T

81465143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: 3 prime UTR variant
orthologous variants: 120182028-A-G

http://identifiers.org/hco/17/GRCh38#81465171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120182051-C-A

81465171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: 3 prime UTR variant
orthologous variants: 120182051-C-T

81465219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: 3 prime UTR variant
orthologous variants: 120182095-A-G

81465268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: 3 prime UTR variant
orthologous variants: 120182143-G-A

81465268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: 3 prime UTR variant
orthologous variants: 120182143-G-T

81465307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: 3 prime UTR variant
orthologous variants: 120182182-G-T

81465634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: 3 prime UTR variant
orthologous variants: 120182393-T-C

81465643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: 3 prime UTR variant
orthologous variants: 120182402-T-C

81465657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: 3 prime UTR variant
orthologous variants: 120182412-A-G

81465667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: 3 prime UTR variant
orthologous variants: 120182422-G-T

81465742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: 3 prime UTR variant
orthologous variants: 120182513-G-T

81465855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: 3 prime UTR variant
orthologous variants: 120182596-T-C

81465899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: 3 prime UTR variant
orthologous variants: 120182639-G-A

81465913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: 3 prime UTR variant
orthologous variants: 120182653-G-A

81465913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: 3 prime UTR variant
orthologous variants: 120182653-G-T

81465978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: 3 prime UTR variant
orthologous variants: 120182720-G-T

81466003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: 3 prime UTR variant
orthologous variants: 120182749-G-T

http://identifiers.org/hco/17/GRCh38#81466031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29279
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120182780-C-A