39665008-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81251205-C-G

39665023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81251220-T-C

39665093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: non coding transcript exon variant
orthologous variants: 81251289-G-T

39665127-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: non coding transcript exon variant
orthologous variants: 81251321-A-T

39665135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: non coding transcript exon variant
orthologous variants: 81251329-G-T

39665271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: non coding transcript exon variant
orthologous variants: 81251445-G-A

39665271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: non coding transcript exon variant
orthologous variants: 81251445-G-T

39665284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: non coding transcript exon variant
orthologous variants: 81251456-G-T

http://identifiers.org/hco/2/GRCh38#39665399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#81251574-C-A

39665399-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81251574-C-G

39665399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81251574-C-T

http://identifiers.org/hco/2/GRCh38#39665471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#81251647-C-A

39665471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81251647-C-T

39665618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81251805-G-A

39665618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81251805-G-T

http://identifiers.org/hco/2/GRCh38#39665624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#81251811-C-A

39665624-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81251811-C-G

39665624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81251811-C-T

39665669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81251869-G-A

39665669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81251869-G-C

39665678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81251879-G-A

39665678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81251879-G-T

39665811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81251970-G-A

39665811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81251970-G-T

39665842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81251986-G-A

39665842-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81251986-G-C

39665842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81251986-G-T

http://identifiers.org/hco/2/GRCh38#39665850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#81251994-C-A

39665850-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81251994-C-G

39665850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81251994-C-T

http://identifiers.org/hco/2/GRCh38#39665853-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#81251997-A-C

http://identifiers.org/hco/2/GRCh38#39665856-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#81252000-A-C

39665874-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81252019-T-G

39665878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81252023-G-A

39665878-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81252023-G-C

39665878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81252023-G-T

http://identifiers.org/hco/2/GRCh38#39665898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#81252042-C-A

39665898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81252042-C-T

39666061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 81252204-C-T

39666215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81252358-G-A

39666215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81252358-G-T

http://identifiers.org/hco/2/GRCh38#39666400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#81252543-C-A

39666400-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81252543-C-G

39666400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81252543-C-T

http://identifiers.org/hco/2/GRCh38#39666455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#81252596-C-A

39666455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81252596-C-G

39666455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81252596-C-T

39666488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81252634-G-A

39666488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81252634-G-T

39666632-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81252760-T-G

39666861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81252973-G-A

39666861-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81252973-G-C

http://identifiers.org/hco/2/GRCh38#39666925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#81253035-C-A

39667447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81253487-G-A

39667447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81253487-G-T

http://identifiers.org/hco/2/GRCh38#39667508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#81253545-C-A

39667508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81253545-C-T

39667844-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81253880-G-C

39667881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81253917-T-C

http://identifiers.org/hco/2/GRCh38#39667984-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#81254019-A-C

39667984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81254019-A-G

39668440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81254490-A-G

39668691-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81254693-T-G

39668841-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81254858-T-A

39668943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81254960-T-C

39669224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81255257-T-C

39669275-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81255308-G-C

39669516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81255510-T-C

39669523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81255536-G-A

39669537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81255577-A-G

http://identifiers.org/hco/2/GRCh38#39669612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#81255650-C-A

39669612-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81255650-C-G

39669612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81255650-C-T

39669821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81256552-T-C

39669974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81256683-T-C

39669974-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81256683-T-G

39669978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81256687-C-T

39670004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81256710-A-G

39670049-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81256964-G-C

39670341-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81257285-T-A

39670441-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81257387-T-A

http://identifiers.org/hco/2/GRCh38#39670565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#81257514-C-A

39670652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81257579-A-G

39671147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81258081-G-T

39671176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81258114-A-G

39671176-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81258114-A-T

39671398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81258352-A-G

39671516-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81258457-G-C

39671531-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81258472-G-C

39671582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81258767-G-T

39671616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81258806-A-G

39671695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81258900-G-A

39671695-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81258900-G-C

39671716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81258921-T-C

39672111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81259331-A-G

39672138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81259359-T-C

39672263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81259484-G-A

39672268-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81259489-T-A

39672415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81259667-G-T

39672876-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81259804-T-A

39673197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81260905-T-C

39673795-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81261480-C-G

39673859-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81261542-C-G

39673887-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81261575-A-T

39674813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81263330-T-C

39675202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81263774-G-A

39675298-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81263880-T-A

39675298-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81263880-T-G

39675441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81264026-A-G

39675467-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81264050-G-C

39675810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81264326-C-T

39675811-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81264327-A-T

39676262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81264559-T-C

39676348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81264645-G-A

39676348-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81264645-G-C

39676450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81264748-G-A

39676501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81264765-C-T

39676594-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81264834-T-G

39676656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81264874-A-G

39676736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81264937-G-A

39676762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81264963-G-A

39676762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81264963-G-T

http://identifiers.org/hco/2/GRCh38#39676845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#81265047-C-A

39676861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81265063-A-G

39677346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81265507-A-G

39677434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81265587-C-T

39677436-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81265589-C-G

39677436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81265589-C-T

39677461-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81265614-T-A

http://identifiers.org/hco/2/GRCh38#39677984-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#81266108-A-C

http://identifiers.org/hco/2/GRCh38#39678554-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#81266644-A-C

39678600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81266683-T-C

39678887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81266966-T-C

39678894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81266973-G-A

39678992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81267066-C-T

http://identifiers.org/hco/2/GRCh38#39679449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#81269268-C-A

39679449-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81269268-C-G

39679692-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81269458-G-C

39679948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81269688-G-A

39679948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81269688-G-T

39679997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81269721-A-G

39680077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81269797-A-G

39680234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81269952-A-G

39680241-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81269959-A-T

39680357-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81270069-G-C

39680410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81270122-G-A

39680595-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81270334-C-G

39680595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81270334-C-T

39680808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81270539-T-C

39680824-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81270555-T-G

http://identifiers.org/hco/2/GRCh38#39681083-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#81270787-A-C

39681601-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81271331-T-G

http://identifiers.org/hco/2/GRCh38#39681671-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#81271382-A-C

39681683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81271394-G-T

39681849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81271562-A-G

39681958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81271658-A-G

39682036-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81271703-T-A

39682084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81271737-C-T

39682125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81271778-G-C

39682130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81271782-G-A

39682155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81271807-C-T

39682167-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81271819-T-G

39682217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81271866-A-G

39682303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81271950-G-A

39682354-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81272008-T-G

39682407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81272065-G-A

39682407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81272065-G-T

39682430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81272085-T-C

http://identifiers.org/hco/2/GRCh38#39682444-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#81272099-A-C

39682482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81272132-C-T

39682537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81272186-A-G

39682594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81272249-C-T

39682699-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81272348-A-T

39682709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81272358-A-G

39682878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81272516-G-A

39682900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81272538-A-G

39683116-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81272729-T-A

39683169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81272812-C-T

39683174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81272817-A-G

39683226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81272869-G-A

39683262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81272905-G-A

39683262-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81272905-G-C

39683266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81273005-G-A

39683272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81273011-A-G

39683344-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81273107-A-T

39683582-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81273566-T-G

39683710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81273695-C-T

39683758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81273725-T-C

39684059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81274350-A-G

http://identifiers.org/hco/2/GRCh38#39684131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#81274422-C-A

39684152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81274442-G-A

39684212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81274507-C-T

39684233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81274526-C-G

http://identifiers.org/hco/2/GRCh38#39684373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#81274673-C-A

39684523-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81274821-T-A

39684572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81274873-T-C

39684703-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81275017-A-T

39685560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81275961-A-G

39685566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81275967-A-G

39685768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81276131-G-A

39685786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81276140-A-G

39685856-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81276208-C-G

39685889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81276248-G-T

39685995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81276612-G-A

39686000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81276621-G-A

39686000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81276621-G-T

39686029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81276650-G-A

39686220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81276860-C-T

39686293-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81276931-C-G

39686513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81277156-G-A

39686561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81277205-T-C

39686674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81277341-G-T

39686702-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81277365-G-C

39686717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81277416-A-G

39686719-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81277418-T-G

39686750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81277450-G-A

39686814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81277515-G-A

39687018-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81277666-T-G

39687312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81277942-A-G

39687495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81278132-G-T

http://identifiers.org/hco/2/GRCh38#39687509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#81278139-C-A

http://identifiers.org/hco/2/GRCh38#39687521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#81278160-C-A

39687521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81278160-C-T

39687561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81278197-T-C

http://identifiers.org/hco/2/GRCh38#39687563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#81278199-C-A

39687563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81278199-C-T

39687566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81278202-C-T

39687568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81278204-T-C

39687630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81278254-A-G

39687654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81278264-T-C

39687683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81278299-C-T

39687705-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81278320-C-G

39687723-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81278338-G-C

39687781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81278393-A-G

39687802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81278414-G-A

http://identifiers.org/hco/2/GRCh38#39687805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#81278417-C-A

39687837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81278449-G-A

39687950-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81278547-G-C

39688118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81278691-C-T

39688141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81278714-C-T

http://identifiers.org/hco/2/GRCh38#39688212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#81278768-C-A

39688376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81278938-A-G

39688451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81279021-G-A

39688492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81279058-A-G

39688535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81279099-C-T

39688786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81279310-A-G

39688846-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81279993-C-G

39688884-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81280029-T-G

39688885-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81280030-A-T

39689003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81280148-C-T

39689080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81280224-C-T

39689267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81280403-G-C

39689352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81280493-A-G

39689543-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81280688-G-C

39689806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81280925-C-T

http://identifiers.org/hco/2/GRCh38#39692333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#81284971-C-A

39692333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81284971-C-T

39692499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81285173-A-G

39692780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81285373-A-G

39692791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81285384-G-A

39692791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81285384-G-T

http://identifiers.org/hco/2/GRCh38#39693273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#81285827-C-A

39693310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81285861-T-C

39693311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81285862-A-G

39693315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81285866-A-G

39693480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81286032-C-T

39693659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81286190-G-A

39693702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81286229-T-C

39693712-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81286239-T-A

39693845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81286514-A-G

39693846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81286515-A-G

39693870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81286539-C-T

39694901-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81287428-T-A

39695308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81287817-T-C

39695705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81288123-G-A

39695725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81288138-G-A

39695725-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81288138-G-C

http://identifiers.org/hco/2/GRCh38#39696184-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#81289185-A-C

39696340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81289337-A-G

39696903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81289867-C-T

39697017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81289980-C-T

http://identifiers.org/hco/2/GRCh38#39697019-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#81289982-A-C

http://identifiers.org/hco/2/GRCh38#39697244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#81290185-C-A

39697259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81290191-T-C

39697489-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81290402-G-C

39697491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81290404-A-G

39697520-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81290433-A-T

39697555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81290469-C-T

http://identifiers.org/hco/2/GRCh38#39697571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#81290485-C-A

39697636-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81290537-A-T

39697671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81290565-G-A

39697671-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81290565-G-C

http://identifiers.org/hco/2/GRCh38#39697677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#81290569-C-A

39697677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81290569-C-T

39697710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81290601-C-T

39697713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81290604-T-C

39697714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81290605-A-G

39697753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81290632-A-G

39697753-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81290632-A-T

39697808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81290683-G-A

39697808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81290683-G-T

http://identifiers.org/hco/2/GRCh38#39697810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#81290685-C-A

39697862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81290737-G-A

39697862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81290737-G-T

http://identifiers.org/hco/2/GRCh38#39697885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#81290758-C-A

39697918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81290792-T-C

39698041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81290970-A-G

39698119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81291052-G-A

39698119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81291052-G-T

39698283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81291188-A-G

39698306-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81291210-T-G

39698360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81291245-G-T

39703048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81292590-A-G

39703057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81292599-T-C

39703082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81292629-G-A

39703084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81292631-A-G

39703100-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81292651-T-G

39703144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81292697-C-T

39703193-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81292786-A-T

39703220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81292812-G-A

39703254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81292844-A-G

39703254-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81292844-A-T

39703420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81292985-G-A

39703422-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81292987-C-G

39703443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81293000-A-G

39703523-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81293035-A-T

39703536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81293048-A-G

39703773-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81293275-A-T

http://identifiers.org/hco/2/GRCh38#39703894-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#81293398-A-C

39703894-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81293398-A-T

39703963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81293489-A-G

39704215-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81293743-T-A

39704251-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81293759-C-G

http://identifiers.org/hco/2/GRCh38#39704254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#81293762-C-A

39704254-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81293762-C-G

39704267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81293774-A-G

39704267-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81293774-A-T

39704309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81293810-G-T

39704367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81293868-G-A

39704427-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81293940-T-A

http://identifiers.org/hco/2/GRCh38#39704449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#81293965-C-A

39704453-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81293969-C-G

39704453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81293969-C-T

39704470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81293989-C-T

http://identifiers.org/hco/2/GRCh38#39704501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#81294082-C-A

39704650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81294395-G-A

39704701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81294453-G-T

39704759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81294511-A-G

39704768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81294520-A-G

39704958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81294706-T-C

39704963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81294711-G-A

39705135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81295269-G-A

39705163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81295296-A-G

39705185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81295321-C-G

39705263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81295399-G-A

39705652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81295983-G-A

39705715-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81296046-T-G

39705722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81296052-G-A

39705722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81296052-G-C

39706457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81296591-G-A

39706498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81296633-A-G

39706509-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81296645-T-G

39706570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81296700-C-T

39706608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81296741-G-A

39706778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81296846-C-T

39706782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81296850-G-A

39706880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81296946-C-T

39706924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81296988-T-C

39707018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81297103-T-C

39707027-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81297112-T-A

39707027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81297112-T-C

39707113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 81297198-T-C

http://identifiers.org/hco/2/GRCh38#39707122-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#81297207-A-C

39707122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 81297207-A-G

http://identifiers.org/hco/2/GRCh38#39707214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#81297299-C-A

39707214-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81297299-C-G

39707460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81297505-T-C

http://identifiers.org/hco/2/GRCh38#39707989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#81297628-C-A

39707989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81297628-C-T

39708057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81297690-T-C

39708077-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81297710-G-C

39708099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81297732-T-C

39708147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81297770-T-C

39708225-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81297848-T-G

39709885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81298685-A-G

39709895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81298695-T-C

39710567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81298882-G-A

39710858-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81299198-C-G

39710974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81299312-C-T

39711212-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81299557-C-G

39711674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81300693-T-C

39711823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81300845-T-C

39711927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81300948-G-A

39712631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81301660-A-G

39713126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81302366-A-G

39713565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81302971-T-C

39713565-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81302971-T-G

39713833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81303229-A-G

39713945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

39714031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

39714407-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: -T-A

39714427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

39714634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81305106-C-T

39714735-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81305184-T-A

39714851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81305285-A-G

39714901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81305357-T-C

39714970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81305426-C-T

39715529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81305953-G-T

39715546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81305969-T-C

39715744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81306335-C-T

39715998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81306529-G-A

39715998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81306529-G-C

39716184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81306727-A-G

39716730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81308047-A-G

39716893-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81308164-T-A

39716893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81308164-T-C

39716895-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81308166-A-T

39716939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81308194-G-A

39716939-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81308194-G-C

39716939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81308194-G-T

39717041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 81308290-T-C

39717062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 81308311-T-C

http://identifiers.org/hco/2/GRCh38#39717345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#81308619-C-A

39717345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 81308619-C-T

39717372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 81308645-G-A

39717372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 81308645-G-T

39717419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 81308692-A-G

39717439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 81308712-T-C

39717470-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 81308739-A-T

http://identifiers.org/hco/2/GRCh38#39717509-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#81308779-A-C

39717509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 81308779-A-G

39717559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 81308830-G-T

http://identifiers.org/hco/2/GRCh38#39717590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#81308861-C-A

39717590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 81308861-C-T

http://identifiers.org/hco/2/GRCh38#39717630-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#81308901-A-C

39717646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 81308917-A-G

39717646-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 81308917-A-T

39717653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 81308924-T-C

39717686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 81308957-G-T

39717770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 81309041-G-A

39717770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 81309041-G-T

39717850-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 81309126-C-G

39717850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 81309126-C-T

http://identifiers.org/hco/2/GRCh38#39717868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#81309142-C-A

39717868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 81309142-C-T

39717869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 81309143-G-A

39717873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 81309147-C-T

39717931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 81309210-G-T

http://identifiers.org/hco/2/GRCh38#39717949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#81309227-C-A

39718170-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron variant
orthologous variants: 81309652-T-G

39718397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28517
most severe consequence: intron variant
orthologous variants: 81309818-A-G