81245420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 119995702-T-C

81245442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 119995724-A-G

81245461-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 119995743-T-A

81245461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 119995743-T-C

81245499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 119995774-G-A

81245499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 119995774-G-T

81245510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 119995785-G-A

http://identifiers.org/hco/17/GRCh38#81245616-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119995883-A-C

81245616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119995883-A-G

http://identifiers.org/hco/17/GRCh38#81245748-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119996015-A-C

81245748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119996015-A-G

81245801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119996068-G-A

81245801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119996068-G-T

81245850-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119996117-G-C

http://identifiers.org/hco/17/GRCh38#81245944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119996208-C-A

81245944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119996208-C-T

81245970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119996237-G-A

81246015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119996252-G-A

81246015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119996252-G-T

81246061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119996295-G-A

81246061-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119996295-G-C

http://identifiers.org/hco/17/GRCh38#81246124-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119996322-A-C

http://identifiers.org/hco/17/GRCh38#81246219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119996405-C-A

81246319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 119996508-T-C

81246329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 119996518-G-A

81246400-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 119996589-T-A

81246400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 119996589-T-C

81246424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 119996613-G-A

81246424-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 119996613-G-C

81246424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 119996613-G-T

81246447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 119996636-G-T

81246511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 119996700-G-T

81246567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 119996756-A-G

81246609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 119996798-G-A

81246609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 119996798-G-T

http://identifiers.org/hco/17/GRCh38#81246612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119996801-C-A

81246612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 119996801-C-T

81246633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 119996822-G-A

81246633-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 119996822-G-C

81246800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119997097-C-T

http://identifiers.org/hco/17/GRCh38#81246868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119997224-C-A

81246868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119997224-C-T

http://identifiers.org/hco/17/GRCh38#81246955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119997330-C-A

81246955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119997330-C-T

81246964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119997339-C-T

81247076-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119997449-C-G

81247076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119997449-C-T

81247098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119997472-T-C

81247134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119997511-C-T

81247137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119997514-C-T

81247138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119997515-A-G

81247184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119997552-G-A

81247184-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119997552-G-C

81247184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119997552-G-T

81247308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119997644-T-C

81247323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119997654-G-A

81247323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119997654-G-T

http://identifiers.org/hco/17/GRCh38#81247335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119997666-C-A

81247335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119997666-C-T

http://identifiers.org/hco/17/GRCh38#81247348-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119997680-A-C

81247348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119997680-A-G

81247377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119997707-G-A

81247377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119997707-G-T

81247516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119997839-G-A

81247516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119997839-G-T

81248794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119998527-A-G

81248887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119998620-G-A

81248941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119998684-C-T

81249106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119998811-G-A

81249599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119998908-G-A

81249599-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119998908-G-C

81249665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119998972-C-T

81249702-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119999002-T-G

81249993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119999220-G-A

81250142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119999365-C-T

http://identifiers.org/hco/17/GRCh38#81250226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119999453-C-A

81250226-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119999453-C-G

81250397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

81250445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-T

81250460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

81250525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

81250814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

81250814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-T

http://identifiers.org/hco/17/GRCh38#81250970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: -C-A

81250970-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: -C-G

81250970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: -C-T

http://identifiers.org/hco/17/GRCh38#81250983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: -C-A

81250983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: -C-T

81251008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119999870-G-T

http://identifiers.org/hco/17/GRCh38#81251228-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: -A-C

81251228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: -A-G

81251252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120000052-G-A

81251275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 120000075-T-C

81251336-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120000137-C-G

81251416-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: -G-C

http://identifiers.org/hco/17/GRCh38#81251418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: -C-A

81251424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120000212-C-T

http://identifiers.org/hco/17/GRCh38#81251448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120000220-C-A

81251448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120000220-C-T

81251487-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120000252-C-G

81251487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120000252-C-T

81251509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120000274-C-T

81251581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120000331-C-T

http://identifiers.org/hco/17/GRCh38#81251590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120000340-C-A

81251590-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120000340-C-G

81251590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120000340-C-T

http://identifiers.org/hco/17/GRCh38#81251605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120000355-C-A

81251605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120000355-C-T

http://identifiers.org/hco/17/GRCh38#81251618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120000368-C-A

81251618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120000368-C-T

81251663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120000409-G-A

81251663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120000409-G-T

http://identifiers.org/hco/17/GRCh38#81251733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120000466-C-A

81251733-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120000466-C-G

81251733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120000466-C-T

81251761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120000494-G-A

81251761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120000494-G-T

81251932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120000662-T-C

81251932-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120000662-T-G

81251954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120000677-G-A

81251954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120000677-G-T

http://identifiers.org/hco/17/GRCh38#81252037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120000760-C-A

81252037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120000760-C-T

http://identifiers.org/hco/17/GRCh38#81252043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120000766-C-A

81252043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120000766-C-T

http://identifiers.org/hco/17/GRCh38#81252115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120000837-C-A

81252135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120000859-C-T

81252168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120000874-C-T

81252224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120000930-G-A

81252224-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120000930-G-C

81252224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120000930-G-T

81252279-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120000970-C-G

81252279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120000970-C-T

81252403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120001094-T-C

81252490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120001169-T-C

81252686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120001365-G-A

81252686-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120001365-G-C

81252686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120001365-G-T

81252704-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120001382-G-C

81252704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120001382-G-T

81252844-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120001500-C-G

81252989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120001592-G-A

81252989-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120001592-G-C

81253164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120001755-C-T

81253240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 120001831-G-A

81253250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120001841-G-A

http://identifiers.org/hco/17/GRCh38#81253343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120001892-C-A

http://identifiers.org/hco/17/GRCh38#81257797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120004929-C-A

81257797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120004929-C-T

81257800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120004932-C-T

81257844-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120004971-C-G

http://identifiers.org/hco/17/GRCh38#81257959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120005094-C-A

81257986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120005121-C-T

81258062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120005200-T-C

81258091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120005229-G-A

http://identifiers.org/hco/17/GRCh38#81258135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120005670-C-A

81258135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120005670-C-T

81258254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120005789-G-A

81258703-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120006278-T-A

81258796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120006349-G-A

81258984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120006550-G-T

81259133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120006699-G-A

81259141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120006707-G-A

81259141-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120006707-G-C

http://identifiers.org/hco/17/GRCh38#81259162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120006733-C-A

81259223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120006789-A-G

81259374-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120006908-C-G

81259642-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120007160-T-G

81259687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120007198-C-T

81259690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120007201-T-C

http://identifiers.org/hco/17/GRCh38#81259978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120007395-C-A

81260096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120007494-G-A

81260110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120007521-C-T

http://identifiers.org/hco/17/GRCh38#81260143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120007555-C-A

81260143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120007555-C-T

http://identifiers.org/hco/17/GRCh38#81260216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120007645-C-A

81260216-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120007645-C-G

81260216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120007645-C-T

81260229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120007674-T-C

http://identifiers.org/hco/17/GRCh38#81260248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120007701-C-A

81260248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120007701-C-T

81260292-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120007745-C-G

81260292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120007745-C-T

http://identifiers.org/hco/17/GRCh38#81260428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120007880-C-A

81260428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120007880-C-T

http://identifiers.org/hco/17/GRCh38#81261817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120008688-C-A

http://identifiers.org/hco/17/GRCh38#81261884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120008735-C-A

81261884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120008735-C-T

81261901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120008748-C-T

81261902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120008749-G-A

81261954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120008809-T-C

81261965-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120008820-A-T

81262131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120008989-G-A

81262294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120009137-C-T

81262768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120009586-C-T

81262808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120009625-A-G

81262870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120009687-A-G

http://identifiers.org/hco/17/GRCh38#81263067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120009971-C-A

81263096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120010025-G-T

81263109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120010054-G-A

81263136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120010090-C-T

81263220-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120010170-G-C

81263234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120010177-C-T

81263343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120010275-C-T

81263376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120010298-A-G

http://identifiers.org/hco/17/GRCh38#81263550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120010426-C-A

81263550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120010426-C-T

81263590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120010455-G-T

http://identifiers.org/hco/17/GRCh38#81263708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120010571-C-A

81263708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120010571-C-T

81263768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120010619-G-T

81263771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120010622-T-C

81263775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120010626-T-C

81263806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120010650-T-C

http://identifiers.org/hco/17/GRCh38#81263837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120010680-C-A

81263837-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120010680-C-G

81263837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120010680-C-T

81263880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120010714-G-A

81263880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120010714-G-T

81264040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120010822-A-G

81264048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120010833-C-T

81264114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120010896-G-A

81264114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120010896-G-T

81264125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120010907-C-T

81264186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120010970-T-C

81264186-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120010970-T-G

http://identifiers.org/hco/17/GRCh38#81264250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120011029-C-A

http://identifiers.org/hco/17/GRCh38#81264255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120011034-C-A

81264255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120011034-C-T

http://identifiers.org/hco/17/GRCh38#81264265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120011044-C-A

81264265-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120011044-C-G

http://identifiers.org/hco/17/GRCh38#81264435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120011213-C-A

81264435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120011213-C-T

81265628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120011936-A-G

81267951-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120013111-C-G

81268219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120013338-A-G

81268271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120013406-C-T

81270148-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120018531-C-G

81270274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120018631-T-C

81270274-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120018631-T-G

http://identifiers.org/hco/17/GRCh38#81270377-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120018699-A-C

81270524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120018846-C-T

81270805-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120019094-T-G

http://identifiers.org/hco/17/GRCh38#81270828-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120019117-A-C

http://identifiers.org/hco/17/GRCh38#81270838-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120019127-A-C

81270868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120019152-A-G

81270896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120019179-C-T

81270972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120019303-G-A

81270972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120019303-G-T

http://identifiers.org/hco/17/GRCh38#81270996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120019327-C-A

81270996-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120019327-C-G

81270996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120019327-C-T

81271086-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120019394-G-C

81271086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120019394-G-T

http://identifiers.org/hco/17/GRCh38#81271097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120019403-C-A

81271097-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120019403-C-G

81271097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120019403-C-T

81271104-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120019410-C-G

81271104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120019410-C-T

http://identifiers.org/hco/17/GRCh38#81271168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120019463-C-A

81271194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120019522-G-A

81271245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120019582-T-C

81271295-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120019633-T-G

81271305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120019643-C-T

81272726-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120020229-A-T

81272736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120020239-G-A

81272736-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120020239-G-C

81272736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120020239-G-T

http://identifiers.org/hco/17/GRCh38#81273056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120020583-C-A

81273063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120020590-A-G

81273103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120020634-C-T

81274141-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120021908-G-C

81274147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120021915-C-T

81274208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120021992-G-A

81274328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120022097-G-A

81276116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120023650-G-A

http://identifiers.org/hco/17/GRCh38#81276205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120023739-C-A

81276205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120023739-C-T

81276217-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120023751-T-A

81276217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120023751-T-C

81276217-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120023751-T-G

81276220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120023754-G-A

81276220-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120023754-G-C

81276220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120023754-G-T

http://identifiers.org/hco/17/GRCh38#81276221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120023755-C-A

81276221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120023755-C-T

81276259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120023818-G-A

81276259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120023818-G-T

81276373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120023999-T-C

http://identifiers.org/hco/17/GRCh38#81276378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120024004-C-A

81276411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120024041-G-A

81276411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120024041-G-T

81276422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120024052-G-T

81276439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120024066-G-A

http://identifiers.org/hco/17/GRCh38#81276499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120024112-C-A

81276517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120024130-G-A

81276547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120024159-A-G

http://identifiers.org/hco/17/GRCh38#81276882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120025470-C-A

81276882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120025470-C-T

http://identifiers.org/hco/17/GRCh38#81276897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120025493-C-A

81276901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120025497-G-A

81276901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120025497-G-T

81276950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120025526-G-A

81276950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120025526-G-T

81276968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120025544-G-T

81276989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120025563-T-C

81277017-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120025592-G-C

81277150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120025725-C-T

81277161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120025734-G-A

81277161-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120025734-G-C

81277161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120025734-G-T

81277190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120025767-G-A

81277283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120025873-G-A

81277283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120025873-G-T

81277358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120025945-T-C

81277461-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120026043-A-T

81277512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120026087-C-T

81277524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120026098-G-A

81277526-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120026100-C-G

81277939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120026443-G-A

81277955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120026465-T-C

81278037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120026543-G-A

http://identifiers.org/hco/17/GRCh38#81278038-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120026544-A-C

81278038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120026544-A-G

81278048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120026600-G-A

81278525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120026934-G-A

81278713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120027101-G-A

81278713-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120027101-G-C

81278740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120027119-C-T

81278772-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120027147-T-G

81279033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120027269-A-G

81279044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120027292-C-T

81279257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120027438-T-C

81279261-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120027442-T-A

81279470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120027630-C-T

http://identifiers.org/hco/17/GRCh38#81279636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120027741-C-A

81279636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120027741-C-T

81279826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120027930-G-A

81279831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120027937-G-A

81279863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120027971-G-A

81279863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120027971-G-T

81279963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120028067-T-C

http://identifiers.org/hco/17/GRCh38#81280001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120028112-C-A

81280001-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120028112-C-G

81280001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120028112-C-T

81280002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120028113-G-A

81280002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120028113-G-C

http://identifiers.org/hco/17/GRCh38#81280038-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120028149-A-C

81280115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120028209-A-G

81280121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120028215-G-A

81280121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120028215-G-T

81280156-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 120028255-G-C

81280162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 120028261-T-C

81280162-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 120028261-T-G

81280191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120028282-G-A

81280278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120028372-T-C

81280762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120028835-G-A

81280762-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120028835-G-C

81280767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120028836-G-A

81280767-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120028836-G-C

81280832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120028883-G-A

81280832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120028883-G-T

81280961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120028989-G-A

81281298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120029149-A-G

81281324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120029175-G-A

http://identifiers.org/hco/17/GRCh38#81281523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120029317-C-A

81281839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120029486-G-A

81282043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120029653-T-C

81282054-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120029662-T-A

81282063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120029671-T-C

81282090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120029722-G-A

http://identifiers.org/hco/17/GRCh38#81282110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120029742-C-A

81282141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120029772-G-A

81282141-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120029772-G-C

81282141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120029772-G-T

81282403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120030022-G-A

81282651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120030305-C-T

81282714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120030648-G-A

81282797-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120030728-T-A

81282845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120030773-C-T

81282878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120030811-G-A

81282895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120030860-G-A

81283170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120031193-C-T

http://identifiers.org/hco/17/GRCh38#81283189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120031223-C-A

81283189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120031223-C-T

http://identifiers.org/hco/17/GRCh38#81283314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120031335-C-A

81283314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120031335-C-T

81283331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120031348-T-C

81283460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120031470-G-A

81284706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120032301-A-G

81284708-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120032303-T-G

81284787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120032356-G-A

81284787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120032356-G-T

81284808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120032384-T-C

81284808-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120032384-T-G

http://identifiers.org/hco/17/GRCh38#81284916-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120032487-A-C

http://identifiers.org/hco/17/GRCh38#81284932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120032503-C-A

81284932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120032503-C-T

81284935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120032518-G-A

81284935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120032518-G-T

81284961-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120032695-T-A

81284961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120032695-T-C

81284961-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120032695-T-G

81284969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120032703-G-T

81284989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120032723-A-G

http://identifiers.org/hco/17/GRCh38#81285010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120032744-C-A

81285010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120032744-C-G

81285010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120032744-C-T

http://identifiers.org/hco/17/GRCh38#81285165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120032924-C-A

81285165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120032924-C-T

81285350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120033183-T-C

81285350-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120033183-T-G

81285358-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120033191-T-A

81285367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120033200-G-T

81285425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120033257-A-G

81285455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120033289-C-T

81285465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120033296-G-A

81285465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120033296-G-T

81285607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120033439-A-G

http://identifiers.org/hco/17/GRCh38#81285770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#120033604-C-A

81285770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, undefined
orthologous variants: 120033604-C-T

81287520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron variant
orthologous variants: 120036194-G-A

http://identifiers.org/hco/17/GRCh38#81287731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120036366-C-A

81287731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron variant
orthologous variants: 120036366-C-T

81287739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron variant
orthologous variants: 120036374-T-C

81287739-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron variant
orthologous variants: 120036374-T-G

81287923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron variant
orthologous variants: 120036561-C-T

http://identifiers.org/hco/17/GRCh38#81287960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120036593-C-A

81288000-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron variant
orthologous variants: 120036641-C-G

http://identifiers.org/hco/17/GRCh38#81288153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120036783-C-A

81288153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron variant
orthologous variants: 120036783-C-T

81288154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron variant
orthologous variants: 120036784-G-A

81288220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron variant
orthologous variants: 120036905-G-A

81288355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron variant
orthologous variants: 120037031-T-C

81288444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron variant
orthologous variants: 120037123-G-A

81288444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron variant
orthologous variants: 120037123-G-C

http://identifiers.org/hco/17/GRCh38#81288514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120037188-C-A

81288514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron variant
orthologous variants: 120037188-C-T

http://identifiers.org/hco/17/GRCh38#81288586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120037264-C-A

81288586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron variant
orthologous variants: 120037264-C-T

http://identifiers.org/hco/17/GRCh38#81288722-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120037379-A-C

81288745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120037403-G-A

81288745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120037403-G-T

81288766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120037423-C-T

81288904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120037558-G-A

81288909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120037563-T-C

81288938-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120037588-G-C

81288943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 120037592-G-T

81288978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120037629-A-G

81288979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120037630-G-T

81288982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120037633-A-G

81288987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120037637-T-C

http://identifiers.org/hco/17/GRCh38#81289063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120037713-C-A

81289063-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120037713-C-G

81289127-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120037775-A-T

81289491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120038338-G-C

81289566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120038391-A-G

http://identifiers.org/hco/17/GRCh38#81289650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120038472-C-A

81289650-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120038472-C-G

81289650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120038472-C-T

81289682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 120038507-G-A

81289886-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120038737-T-A

81289918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120038755-A-G

81289985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120038823-G-A

81289986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120038824-C-T

81290074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120038862-G-A

81290198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120038980-C-T

81290281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120039054-G-A

81290522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120039241-G-A

http://identifiers.org/hco/17/GRCh38#81292732-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120040681-A-C

81292732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120040681-A-G

81292766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120040706-C-T

81293423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120041031-A-G

81294938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 120041920-G-A

http://identifiers.org/hco/17/GRCh38#81294946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120041928-C-A

81294946-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 120041928-C-G

81294946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 120041928-C-T

81295070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 120041956-G-A

81295070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 120041956-G-T

http://identifiers.org/hco/17/GRCh38#81295223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#120042058-C-A

http://identifiers.org/hco/17/GRCh38#81295283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#120042124-C-A

81295283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 120042124-C-T

81295293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 120042132-G-A

81295293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 120042132-G-T

81295305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 120042144-T-C

http://identifiers.org/hco/17/GRCh38#81295315-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#120042153-A-C

81295315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, undefined
orthologous variants: 120042153-A-G

81295319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, undefined
orthologous variants: 120042157-G-A

81295319-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, undefined
orthologous variants: 120042157-G-C

81295319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, undefined
orthologous variants: 120042157-G-T

http://identifiers.org/hco/17/GRCh38#81295374-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#120042214-A-C

http://identifiers.org/hco/17/GRCh38#81295396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#120042244-C-A

81295396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: intron_variant, undefined
orthologous variants: 120042244-C-T

81295478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 120042395-G-A

81295478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 120042395-G-T

81295532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28237
most severe consequence: 5 prime UTR variant
orthologous variants: 120042437-T-C