http://identifiers.org/hco/17/GRCh38#68975392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/11/GRCm39#109992377-C-A

http://identifiers.org/hco/17/GRCh38#68975426-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109992408-A-C

68975426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109992408-A-G

68975426-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109992408-A-T

http://identifiers.org/hco/17/GRCh38#68975430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109992412-C-A

68975430-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109992412-C-G

68975431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109992413-A-G

68975440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109992422-A-G

68975593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109992570-G-A

68975593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109992570-G-C

68975593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109992570-G-T

68975606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109992583-G-T

http://identifiers.org/hco/17/GRCh38#68975642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109992616-C-A

68975642-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109992616-C-G

68975646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109992620-A-G

68975656-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109992630-T-A

68975676-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109992650-G-C

68975710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109992669-G-A

68975710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109992669-G-T

http://identifiers.org/hco/17/GRCh38#68975724-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109992683-A-C

68975724-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109992683-A-T

http://identifiers.org/hco/17/GRCh38#68975858-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109992734-A-C

68975860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109992736-A-G

http://identifiers.org/hco/17/GRCh38#68975881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109992759-C-A

68975882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109992760-A-G

68975882-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109992760-A-T

68975912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109992788-G-A

http://identifiers.org/hco/17/GRCh38#68975918-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109992794-A-C

68975921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 109992797-C-T

68975958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 109992834-T-C

68976029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109992918-G-T

http://identifiers.org/hco/17/GRCh38#68976077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109992966-C-A

68976077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109992966-C-T

68976203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109993405-G-A

68976215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109993417-G-A

http://identifiers.org/hco/17/GRCh38#68976221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109993424-C-A

http://identifiers.org/hco/17/GRCh38#68976258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109993461-C-A

68976313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109993507-A-G

http://identifiers.org/hco/17/GRCh38#68976335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109993531-C-A

68976335-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109993531-C-G

68976335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109993531-C-T

68976338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109993534-G-A

68976338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109993534-G-T

68976507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109993699-C-T

68976550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109993742-T-C

68976554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109993746-G-A

68977652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109994450-G-A

68977811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109994574-C-T

http://identifiers.org/hco/17/GRCh38#68981462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109994826-C-A

http://identifiers.org/hco/17/GRCh38#68981528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109994885-C-A

68981528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109994885-C-T

http://identifiers.org/hco/17/GRCh38#68982435-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109997252-A-C

68982435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109997252-A-G

68982435-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109997252-A-T

68982465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109997282-C-T

68982510-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109997309-G-C

68982510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109997309-G-T

http://identifiers.org/hco/17/GRCh38#68982597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109997385-C-A

68982597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 109997385-C-T

http://identifiers.org/hco/17/GRCh38#68982602-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109997390-A-C

68982646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 109997434-G-A

68982646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 109997434-G-T

68982689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109997474-A-G

http://identifiers.org/hco/17/GRCh38#68982693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109997478-C-A

68982693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109997478-C-T

68982694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109997479-G-A

68983112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109997573-T-C

68983559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109997799-G-A

68983559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109997799-G-T

68983561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109997801-G-A

68983561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109997801-G-T

68983583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109997828-T-C

http://identifiers.org/hco/17/GRCh38#68983620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109997865-C-A

68983620-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109997865-C-G

68983620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109997865-C-T

68983771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 109998018-T-C

http://identifiers.org/hco/17/GRCh38#68983891-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109998142-A-C

68983920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109998171-G-A

68983968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109998220-C-T

68984006-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109998243-C-G

68984027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109998263-G-T

68984037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109998273-G-A

68984042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109998277-G-T

68984060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 109998295-G-A

68984106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 109998341-C-T

http://identifiers.org/hco/17/GRCh38#68984163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109998398-C-A

68984163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 109998398-C-T

68984423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109998669-G-A

68984466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109998705-G-T

68984551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109998779-A-G

68984560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109998788-G-A

68984569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109998797-T-C

68984588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109998816-A-G

68984642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109998864-G-A

68984755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109999351-A-G

68984780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109999373-T-C

68984782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109999375-C-T

68984785-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109999378-G-C

68984785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109999378-G-T

68984827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109999423-G-T

68984854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109999450-C-T

68984855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109999451-A-G

68984905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 109999498-G-A

68984977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 109999570-C-T

http://identifiers.org/hco/17/GRCh38#68985138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109999732-A-C

http://identifiers.org/hco/17/GRCh38#68985169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109999767-C-A

68985169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109999767-C-T

68985170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109999768-G-A

68985170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109999768-G-T

68985212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109999800-G-T

http://identifiers.org/hco/17/GRCh38#68985967-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110000921-A-C

68986037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110000988-T-C

68986038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110000989-A-G

68986039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110000990-G-A

68986039-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110000990-G-C

68986039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110000990-G-T

68986042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110000993-G-T

http://identifiers.org/hco/17/GRCh38#68986045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110000996-C-A

68986045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110000996-C-T

68986101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110001049-G-T

68986145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110001096-G-A

http://identifiers.org/hco/17/GRCh38#68986157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110001106-C-A

68986157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 110001106-C-T

http://identifiers.org/hco/17/GRCh38#68986158-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110001107-A-C

68986158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110001107-A-G

68986286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 110001235-G-A

http://identifiers.org/hco/17/GRCh38#68986373-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110001317-A-C

68986373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110001317-A-G

68986405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110001345-G-A

68986405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110001345-G-T

68986476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110001904-G-T

68986478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110001906-T-C

68986523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110001958-T-C

68986523-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110001958-T-G

68986611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110002046-A-G

http://identifiers.org/hco/17/GRCh38#68986618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110002053-C-A

68986618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110002053-C-T

http://identifiers.org/hco/17/GRCh38#68986619-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110002054-A-C

68986619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110002054-A-G

68986774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110002166-T-C

http://identifiers.org/hco/17/GRCh38#68986870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110002259-C-A

68986870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110002259-C-T

68986917-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110002295-A-T

http://identifiers.org/hco/17/GRCh38#68987207-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110002563-A-C

68987249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110002605-C-T

68987346-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110002695-G-C

68987504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110002839-A-G

68987598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110002917-C-T

68988119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110003110-G-T

http://identifiers.org/hco/17/GRCh38#68988274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110003266-C-A

68988407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110003371-A-G

68988487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110003463-G-A

68988691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110003646-C-T

68988776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110003765-G-T

68988778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110003767-C-T

68988854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110003842-C-T

68988916-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110003896-T-G

68988947-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110003925-A-T

68989013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110004004-T-C

http://identifiers.org/hco/17/GRCh38#68989242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110004267-C-A

68989242-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110004267-C-G

68989242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110004267-C-T

68989250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110004275-T-C

68989254-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110004279-T-A

http://identifiers.org/hco/17/GRCh38#68989278-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110004303-A-C

68989278-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110004303-A-T

68989418-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110004438-A-T

68989669-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110004889-T-G

68989697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110004917-A-G

http://identifiers.org/hco/17/GRCh38#68989706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110004939-C-A

68989706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110004939-C-T

68989860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110005097-C-T

68989928-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 110005165-T-G

68989969-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110005208-A-T

http://identifiers.org/hco/17/GRCh38#68989993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110005231-C-A

68990001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110005239-T-C

68990223-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110005474-C-G

68990223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110005474-C-T

68990244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110005496-C-T

68990655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110006101-T-C

68990677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110006123-T-C

68990689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110006134-G-A

68990689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110006134-G-T

68990777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110006225-G-A

68990777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110006225-G-T

http://identifiers.org/hco/17/GRCh38#68990785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110006233-C-A

68990807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110006248-T-C

68990807-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110006248-T-G

68990820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110006253-A-G

68990847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110006280-T-C

68990864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 110006297-A-G

68990913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110006346-G-A

68990913-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110006346-G-C

68991087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110006447-T-C

68991087-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110006447-T-G

http://identifiers.org/hco/17/GRCh38#68991096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110006455-C-A

68991096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110006455-C-T

http://identifiers.org/hco/17/GRCh38#68991097-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110006456-A-C

68991097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110006456-A-G

68991097-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110006456-A-T

68991543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110006879-G-A

68991573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110006907-C-T

68991674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110007389-T-C

68991674-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110007389-T-G

68991724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110007439-T-C

68992037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110007749-G-T

68992051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110007763-G-C

68992051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110007763-G-T

68992056-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110007770-T-A

http://identifiers.org/hco/17/GRCh38#68992088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110007799-C-A

68992107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110007819-G-A

68992107-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110007819-G-C

68992107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110007819-G-T

http://identifiers.org/hco/17/GRCh38#68992110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110007822-C-A

68992110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110007822-C-T

68992167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 110007877-T-C

68992251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110007961-G-A

68992255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 110007965-A-G

http://identifiers.org/hco/17/GRCh38#68992290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110008000-C-A

68992290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110008000-C-T

68992328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110008038-G-A

68992328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110008038-G-T

68992853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110008746-G-A

68992853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110008746-G-T

68992879-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110008772-A-T

68993005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110008896-A-G

68993005-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110008896-A-T

68993054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110008945-C-T

68993076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 110008967-A-G

68993076-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 110008967-A-T

68993120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110009008-T-C

68993131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110009016-T-C

http://identifiers.org/hco/17/GRCh38#68993147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110009030-C-A

68993147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110009030-C-T

http://identifiers.org/hco/17/GRCh38#68993166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110009045-C-A

68993213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110009062-T-C

68993213-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110009062-T-G

http://identifiers.org/hco/17/GRCh38#68993214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110009063-C-A

68993223-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110009072-G-C

68993223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110009072-G-T

68993245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110009092-T-C

68993367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110009133-T-C

68993392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110009157-C-T

68993398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110009163-C-T

68995541-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110011146-T-A

68995541-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110011146-T-G

68995611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110011206-G-A

68995685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110011270-G-A

68995708-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110011292-C-G

68995741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110011326-C-T

68995760-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110011346-G-C

68995760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110011346-G-T

68995784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110011370-G-A

68995784-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110011370-G-C

68995786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110011374-C-T

68995827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110011425-G-T

68995851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110011449-G-T

68995880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110011475-A-G

68995898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 110011493-A-G

68995966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110011561-G-T

68995973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 110011568-A-G

68995988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 110011583-A-G

68996032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110011627-T-C

68996033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110011628-A-G

68996043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110011638-T-C

68996044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110011639-A-G

http://identifiers.org/hco/17/GRCh38#68996054-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110011649-A-C

68996054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110011649-A-G

68996059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110011654-G-A

68996059-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110011654-G-C

68996059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110011654-G-T

68996108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110011684-T-C

68996137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110011707-A-G

68996157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110011717-T-C

68996301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110011823-T-C

68996302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110011824-G-A

68996627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110013600-A-G

68996695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110013639-G-A

68996812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110013753-C-T

68996921-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110013844-A-T

69007605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110017765-T-C

69007855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 110018283-G-A

69007855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 110018283-G-T

69007933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110018353-T-C

http://identifiers.org/hco/17/GRCh38#69007940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110018360-C-A

69007940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110018360-C-T

69007945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110018365-T-C

69007998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110021309-A-G

http://identifiers.org/hco/17/GRCh38#69008015-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110021326-A-C

69008015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110021326-A-G

69008023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110021335-A-G

http://identifiers.org/hco/17/GRCh38#69008028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110021340-C-A

http://identifiers.org/hco/17/GRCh38#69008281-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110021640-A-C

69008300-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110021657-A-T

69008350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110021706-C-T

69008367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110021723-A-G

69008406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110021763-T-C

http://identifiers.org/hco/17/GRCh38#69011851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110022479-C-A

69011870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110022498-A-G

69011889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110022517-A-G

69012048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 110022665-G-A

69012048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110022665-G-T

69012063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 110022680-A-G

http://identifiers.org/hco/17/GRCh38#69012193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110022790-C-A

69012202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110022799-G-T

69012207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110022804-A-G

69013973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110023454-C-T

http://identifiers.org/hco/17/GRCh38#69015557-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110024499-A-C

69015569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110024511-G-A

69015726-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110024660-A-T

69015827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110024764-C-T

http://identifiers.org/hco/17/GRCh38#69015921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110024832-C-A

69016092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110024897-A-G

69016265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 110025018-G-A

69016376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 110025129-T-C

69016389-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 110025142-T-A

69016411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110025164-A-G

69016491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110025242-A-G

http://identifiers.org/hco/17/GRCh38#69016515-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110025261-A-C

69017236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110025773-A-G

69017304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110025856-T-C

69017304-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110025856-T-G

69017378-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110025929-T-G

69017505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110026010-G-A

69017505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110026010-G-T

69017554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110026058-T-C

69017554-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110026058-T-G

69017565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110026065-A-G

69017577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110026077-A-G

69017592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110026093-A-G

69017600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110026101-A-G

69017607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110026108-C-T

http://identifiers.org/hco/17/GRCh38#69017609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110026110-C-A

69017609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110026110-C-T

69017610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110026111-C-T

69017637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110026142-C-T

69017695-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 110026200-T-A

69017695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 110026200-T-C

69017783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110026288-G-A

69017783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110026288-G-T

69017795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 110026301-T-C

69017819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110026328-A-G

69017861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110026365-T-C

69017901-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110026398-G-C

69017901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110026398-G-T

69017926-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110026422-T-A

69017926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110026422-T-C

http://identifiers.org/hco/17/GRCh38#69017955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110026450-C-A

69017958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110026453-A-G

http://identifiers.org/hco/17/GRCh38#69017987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110026482-C-A

69017993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110026486-A-G

69018225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110026711-G-T

http://identifiers.org/hco/17/GRCh38#69018250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110026736-C-A

69018250-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110026736-C-G

69018251-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110026737-T-A

69018251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110026737-T-C

69018354-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110026823-T-G

69018646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110027107-G-A

69018646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110027107-G-T

69018666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110027132-A-G

69018669-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110027135-A-T

69018700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110027151-A-G

69018710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110027159-G-A

69018710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110027159-G-T

http://identifiers.org/hco/17/GRCh38#69019937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110028557-C-A

69019983-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110028601-A-T

69020009-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110028676-A-T

69020219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110028841-A-G

http://identifiers.org/hco/17/GRCh38#69020374-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110028949-A-C

69020438-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 110029010-T-G

69020483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 110029055-T-C

69020483-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 110029055-T-G

69020523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110029092-A-G

http://identifiers.org/hco/17/GRCh38#69020529-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110029098-A-C

69020568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110029137-T-C

69020568-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110029137-T-G

69020686-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110029256-T-A

69020686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110029256-T-C

69020692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110029262-G-T

http://identifiers.org/hco/17/GRCh38#69020709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110029275-C-A

69020738-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110029304-T-A

69020738-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110029304-T-G

69020743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110029309-A-G

69020753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110029319-G-A

69020780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110029346-G-A

69020780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110029346-G-T

69020797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110029364-T-C

69020798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110029365-G-T

http://identifiers.org/hco/17/GRCh38#69020823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110029382-C-A

69020878-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110029431-A-T

69020882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110029435-A-G

69020922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110029476-G-A

69020922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110029476-G-T

69020954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110029508-C-T

69021321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110030048-C-T

69021337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110030062-G-A

69021365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110030086-T-C

69021400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110030121-A-G

69021634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110030318-T-C

69021800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110030403-T-C

69021800-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 110030403-T-G

69021936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110030544-A-G

69021958-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110030568-T-A

69022010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110030620-A-G

69022041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110030652-T-C

69022732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110031482-C-T

69022763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110031513-C-T

69022785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110031538-A-G

69022951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110031696-C-T

69023035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110031772-A-G

http://identifiers.org/hco/17/GRCh38#69023060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110031797-C-A

http://identifiers.org/hco/17/GRCh38#69023069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110031812-C-A

69023199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 110032107-G-A

69023243-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110032149-T-G

69023300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110032211-C-T

69024272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 110032393-T-C

69024292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110032413-A-G

69024311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 110032432-T-C

69024327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110032448-G-A

http://identifiers.org/hco/17/GRCh38#69024331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110032452-C-A

69024331-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110032452-C-G

http://identifiers.org/hco/17/GRCh38#69024335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110032456-C-A

69024335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 110032456-C-T

69024342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110032463-T-C

69024370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110032491-A-G

http://identifiers.org/hco/17/GRCh38#69024405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110032516-C-A

69024405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110032516-C-T

http://identifiers.org/hco/17/GRCh38#69024470-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110032575-A-C

69024477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110032582-T-C

http://identifiers.org/hco/17/GRCh38#69024490-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110032595-A-C

http://identifiers.org/hco/17/GRCh38#69024500-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110032605-A-C

69024500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110032605-A-G

69024529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110032626-G-A

69024530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110032627-C-T

69024832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110033601-A-G

69025005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110033777-T-C

69025071-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110033833-T-G

69025167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110033931-A-G

http://identifiers.org/hco/17/GRCh38#69025255-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110034020-A-C

69025258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110034023-A-G

69025352-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110034106-C-G

69025352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110034106-C-T

http://identifiers.org/hco/17/GRCh38#69025997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110034676-C-A

69026027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110034705-G-A

69026089-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110034765-G-C

69026193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110034853-C-T

69026308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110034960-G-A

69026308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110034960-G-T

http://identifiers.org/hco/17/GRCh38#69026318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110034970-C-A

69026318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110034970-C-T

69026340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110034992-G-A

69026340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110034992-G-T

69026475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 110035123-G-A

69026475-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 110035123-G-C

http://identifiers.org/hco/17/GRCh38#69026543-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110035195-A-C

69026543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110035195-A-G

69026549-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110035201-T-A

69026563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110035217-G-T

http://identifiers.org/hco/17/GRCh38#69026565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110035219-C-A

69026565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110035219-C-T

http://identifiers.org/hco/17/GRCh38#69026591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110035231-C-A

69026613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110035240-T-C

69026613-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110035240-T-G

69026616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110035243-T-C

69026646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110035269-A-G

69026650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110035273-T-C

69026650-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110035273-T-G

69026669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110035291-G-A

69026696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110035318-G-T

69026730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110035351-T-C

69026754-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110035375-T-A

69026870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110035466-T-C

69026874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110035469-G-A

69026874-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110035469-G-C

69026874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110035469-G-T

69026910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110035506-T-C

69026926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110035518-A-G

69027033-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110035626-A-T

69027097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 110035690-T-C

69027106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 110035699-T-C

69027109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 110035702-C-T

69027122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 110035715-G-A

69027155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110035751-G-A

69027189-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110035785-A-T

69027271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110035847-T-C

69027519-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110036189-T-G

69027609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110036286-T-C

69027624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110036301-T-C

http://identifiers.org/hco/17/GRCh38#69027663-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110036340-A-C

69027733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 110036410-T-C

69027754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 110036431-C-T

69027762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110036439-T-C

69028080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

http://identifiers.org/hco/17/GRCh38#69028108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-A

69028108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

69028540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110037739-G-A

69028540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110037739-G-T

69028678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110037876-G-A

69028678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110037876-G-T

http://identifiers.org/hco/17/GRCh38#69028679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110037877-C-A

69028694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110037892-T-C

69028694-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110037892-T-G

http://identifiers.org/hco/17/GRCh38#69028753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110037950-C-A

69029126-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110038017-A-T

69029329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110038175-G-A

69029329-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110038175-G-C

69029329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110038175-G-T

69029339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110038185-T-C

69029363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110038189-G-A

69029387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110038213-A-G

http://identifiers.org/hco/17/GRCh38#69029410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110038236-C-A

69029410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110038236-C-T

http://identifiers.org/hco/17/GRCh38#69029498-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110038325-A-C

69029753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110038535-C-T

69029785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110038562-T-C

69029868-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110038634-A-T

69031583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110038985-A-G

69031583-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110038985-A-T

69031802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110039249-A-G

69031879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110039318-C-T

69031893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110039348-T-C

69031964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110039419-G-A

69031964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110039419-G-T

http://identifiers.org/hco/17/GRCh38#69031986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110039441-C-A

69031986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110039441-C-T

69032011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110039466-G-A

69032011-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110039466-G-C

69032011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110039466-G-T

69032071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110039527-G-A

69032071-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110039527-G-C

69032343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110039813-G-A

69032377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110039847-T-C

http://identifiers.org/hco/17/GRCh38#69032513-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110039921-A-C

69032530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110039934-G-A

69033726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 110042772-C-T

http://identifiers.org/hco/17/GRCh38#69033946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110042989-C-A

69033965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110043006-G-A

69033965-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110043006-G-C

69034099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110043084-A-G

69034153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110043135-T-C

69034725-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110043266-G-C

69034770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110043308-T-C

69034934-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110043397-T-G

69035023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110043478-A-G

http://identifiers.org/hco/17/GRCh38#69035052-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110043506-A-C

69035054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110043508-G-T

69035077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

69035169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

69035169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-T

69035176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

69035176-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-C

69035176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-T

http://identifiers.org/hco/17/GRCh38#69035198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-A

69035198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-G

69035327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 110045285-T-C

69035371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110045329-C-T

69035472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110045428-G-A

http://identifiers.org/hco/17/GRCh38#69035485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110045441-C-A

69035485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110045441-C-T

http://identifiers.org/hco/17/GRCh38#69035791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110046112-C-A

69035856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110046176-A-G

http://identifiers.org/hco/17/GRCh38#69035975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110046302-C-A

69040731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110047040-A-G

69040977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110047248-T-C

69040984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110047255-T-C

69042229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110048355-T-C

69042356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110048476-A-G

69042541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110048651-G-T

69042608-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110048714-A-T

69042694-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110048808-T-A

69042694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110048808-T-C

69042694-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110048808-T-G

69043424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110048941-G-A

69043424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110048941-G-T

69043430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110048947-A-G

http://identifiers.org/hco/17/GRCh38#69043431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110048949-C-A

69043431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110048949-C-T

69043437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110048955-A-G

69043457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110048975-G-T

69043459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110048977-T-C

69043459-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110048977-T-G

69043460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110048978-G-A

69043473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110048991-G-A

69043473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110048991-G-T

69043482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 110049000-G-T

69043558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110049076-T-C

69043711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110049229-G-T

http://identifiers.org/hco/17/GRCh38#69043862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110049316-C-A

69043864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110049318-G-A

69043864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110049318-G-T

http://identifiers.org/hco/17/GRCh38#69043866-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110049320-A-C

69043915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110049353-G-A

69044023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110049461-C-T

69044244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110049485-A-G

69044357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110049602-A-G

http://identifiers.org/hco/17/GRCh38#69044380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110049625-C-A

69044380-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110049625-C-G

http://identifiers.org/hco/17/GRCh38#69044457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110049738-C-A

69044468-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110049750-T-G

69044712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110049991-T-C

69044762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110050039-G-A

69044839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110050116-G-A

69044839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110050116-G-T

69045194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110051248-C-T

http://identifiers.org/hco/17/GRCh38#69045195-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110051249-A-C

69045195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110051249-A-G

http://identifiers.org/hco/17/GRCh38#69045322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110051376-C-A

69045326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 110051380-G-T

69045328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110051382-T-C

69045388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110051449-G-A

69045418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110051479-A-G

69046233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110052022-C-G

http://identifiers.org/hco/17/GRCh38#69046358-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110052174-A-C

69046502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110052310-G-A

69046502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110052310-G-T

69046563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110052371-T-C

69048966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110053678-G-T

69049084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110053793-C-T

69049158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110053865-A-G

69049158-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110053865-A-T

69049171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110053878-G-T

69049173-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110053880-T-A

69049211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110053918-T-C

http://identifiers.org/hco/17/GRCh38#69049256-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110053968-A-C

69049256-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110053968-A-T

http://identifiers.org/hco/17/GRCh38#69049260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110053972-C-A

69049260-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110053972-C-G

69049260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110053972-C-T

http://identifiers.org/hco/17/GRCh38#69049387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110054101-C-A

69049387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110054101-C-T

69049388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110054102-G-A

69049388-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110054102-G-C

69049417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110054131-G-A

69049417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110054131-G-T

69049418-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110054132-T-A

69049523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110054249-T-C

69049523-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110054249-T-G

69049526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110054252-T-C

69049563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110054274-T-C

69049577-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110054288-T-A

http://identifiers.org/hco/17/GRCh38#69049589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110054300-C-A

69049589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110054300-C-T

69049615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110054350-A-G

69049615-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110054350-A-T

69049631-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110054364-G-C

69049631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110054364-G-T

69050006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110054910-T-C

69050036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110054926-T-C

69050192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110055144-A-G

69050228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110055183-C-T

69050266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110055224-A-G

69050389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110055306-G-A

69050826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110056531-C-T

69050895-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110056590-T-A

69050895-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110056590-T-G

69050896-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110056591-T-G

http://identifiers.org/hco/17/GRCh38#69050938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110056624-C-A

http://identifiers.org/hco/17/GRCh38#69050973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110056663-C-A

69050973-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110056663-C-G

69050973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110056663-C-T

69051012-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110056704-C-G

69051013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110056705-A-G

69051020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110056712-C-T

69051197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110056887-G-A

69051197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110056887-G-T

69051233-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110056923-T-G

69051244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110056934-A-G

69051244-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110056934-A-T

69051251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110056941-G-A

69051251-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110056941-G-C

69051251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110056941-G-T

http://identifiers.org/hco/17/GRCh38#69051280-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110056978-A-C

69051313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110057010-G-T

69051550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110057203-T-C

http://identifiers.org/hco/17/GRCh38#69051552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110057205-C-A

http://identifiers.org/hco/17/GRCh38#69051620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110057250-C-A

69051632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110057262-G-A

69051632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110057262-G-T

69051641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110057271-G-A

http://identifiers.org/hco/17/GRCh38#69051707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110057325-C-A

http://identifiers.org/hco/17/GRCh38#69051718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110057336-C-A

69051718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110057336-C-T

69051749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110057367-A-G

69051754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 110057372-A-G

69051782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110057395-A-G

69051907-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110057521-C-G

69060213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110058143-A-G

http://identifiers.org/hco/17/GRCh38#69060510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110058405-C-A

69060646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110058555-G-A

http://identifiers.org/hco/17/GRCh38#69060798-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110058708-A-C

69060798-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110058708-A-T

http://identifiers.org/hco/17/GRCh38#69078758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110067608-C-A

69078850-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 110067686-A-T