39048788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31120798-T-C

http://identifiers.org/hco/6/GRCh38#39048837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31120847-C-A

39048837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31120847-C-T

http://identifiers.org/hco/6/GRCh38#39048839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31120849-C-A

39048839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31120849-C-T

http://identifiers.org/hco/6/GRCh38#39048845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31120855-C-A

39048845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31120855-C-T

39048929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31120939-G-A

39048929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31120939-G-T

39048931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31120941-G-A

39048931-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31120941-G-C

39048931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31120941-G-T

39048960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31120969-G-A

39048960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31120969-G-T

http://identifiers.org/hco/6/GRCh38#39048961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31120970-C-A

39048961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31120970-C-T

39049011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31121021-C-T

39049055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31121064-G-A

39049055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31121064-G-T

39049725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31121670-A-G

39049786-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31121739-G-C

39049858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31121809-G-A

http://identifiers.org/hco/6/GRCh38#39049908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31121856-C-A

http://identifiers.org/hco/6/GRCh38#39049976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31121921-C-A

http://identifiers.org/hco/6/GRCh38#39050095-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31122027-A-C

http://identifiers.org/hco/6/GRCh38#39050174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31122091-C-A

39050174-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31122091-C-G

39050314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31122205-A-G

39050367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31122256-A-G

39050701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31122561-C-T

39050821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31122658-G-A

http://identifiers.org/hco/6/GRCh38#39050823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31122660-C-A

39050911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31122749-C-T

http://identifiers.org/hco/6/GRCh38#39051131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31122951-C-A

39051211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31123031-A-G

http://identifiers.org/hco/6/GRCh38#39051472-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31123273-A-C

39051495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31123296-C-T

http://identifiers.org/hco/6/GRCh38#39051537-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31123337-A-C

39051559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31123359-C-T

39051715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31123509-T-C

39051742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31123537-G-T

39051745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31123540-T-C

http://identifiers.org/hco/6/GRCh38#39051823-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31123615-A-C

39051823-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31123615-A-T

39051838-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31123630-T-G

39051889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31123710-G-T

39051911-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31123723-T-G

39053954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31124755-T-C

http://identifiers.org/hco/6/GRCh38#39054060-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31124835-A-C

39054094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31124859-T-C

39054155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31124916-T-C

39054599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31125143-C-T

39054633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31125177-G-A

39054885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31125419-T-C

39054886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31125420-G-T

http://identifiers.org/hco/6/GRCh38#39054981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31125508-C-A

39055073-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31125615-C-G

39055186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31125904-C-T

39055201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31125915-C-T

39055267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31126001-T-C

39055370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31126120-A-G

39055525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31126268-C-T

39055568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31126304-A-G

39055684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31126421-A-G

39055684-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31126421-A-T

39055721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31126455-A-G

39055721-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31126455-A-T

39055763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31126492-G-A

39055819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31126545-G-A

39055819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31126545-G-T

39056008-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31126707-C-G

39056018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31126717-G-A

39056072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31126796-T-C

39056301-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31126995-T-G

39056313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31127007-G-T

39056354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31127046-G-A

39056354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31127046-G-T

http://identifiers.org/hco/6/GRCh38#39056369-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31127060-A-C

39056369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31127060-A-G

39056369-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31127060-A-T

http://identifiers.org/hco/6/GRCh38#39056450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31127148-C-A

39056461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31127159-G-A

39056497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31127195-A-G

http://identifiers.org/hco/6/GRCh38#39056535-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31127226-A-C

http://identifiers.org/hco/6/GRCh38#39056537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31127228-C-A

http://identifiers.org/hco/6/GRCh38#39056570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31127260-C-A

39056570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31127260-C-T

39056601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31127290-T-C

http://identifiers.org/hco/6/GRCh38#39056940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31127703-C-A

39056945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31127708-A-G

39056952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31127715-T-C

39056953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31127716-A-G

39057010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31127773-C-T

39057230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31127974-A-G

39057270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31128013-T-C

39057369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31128108-G-T

http://identifiers.org/hco/6/GRCh38#39057377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31128118-C-A

39057377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31128118-C-T

39057379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31128120-G-A

39057379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31128120-G-T

http://identifiers.org/hco/6/GRCh38#39057473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31128199-C-A

39057548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31128274-C-T

39057938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31128352-C-T

39057946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31128360-C-T

39058062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31128473-G-A

39058063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31128474-C-T

39058164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31128554-T-C

39058164-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31128554-T-G

39058203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31128596-G-T

39058347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31128866-G-A

39058783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31129546-C-T

39058943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31129673-G-A

39059143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31129826-G-A

39059260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31129946-T-C

39059278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31129969-A-G

39059371-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31130083-A-T

39059482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31130188-A-G

39059485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31130191-G-A

39059504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31130210-C-T

39059594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31130315-T-C

39059637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31130381-C-G

39059637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31130381-C-T

39059692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31130433-C-T

39059782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31130517-G-A

39059845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31130578-C-T

39059989-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31130713-C-G

39060032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31130763-G-A

39060047-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31130777-C-G

39060047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31130777-C-T

39060118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31130839-G-A

39060226-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31130907-A-T

39060292-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31130974-T-G

39060739-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31131310-T-A

http://identifiers.org/hco/6/GRCh38#39061005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31131532-C-A

39061037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31131563-A-G

39061096-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31131611-G-C

39061138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31131658-G-A

39061227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31131738-C-T

39061385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31131887-C-T

39061660-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31132107-T-A

39061880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31132313-C-T

39062107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31132541-G-A

39062139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31132573-G-A

39062271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31132704-T-C

39062405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31132837-A-G

39062988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31133336-G-A

39063045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31133457-A-G

39063092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31133534-G-T

http://identifiers.org/hco/6/GRCh38#39063667-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31134537-A-C

39063681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31134554-G-A

39065088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31136910-G-T

39065094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31136916-T-C

39065104-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31136936-T-A

39065141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31136985-C-T

39065210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31137057-C-T

39065237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31137085-C-T

39065287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31137136-G-T

39065404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31137251-G-A

http://identifiers.org/hco/6/GRCh38#39065476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31137321-C-A

39065476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31137321-C-T

http://identifiers.org/hco/6/GRCh38#39065669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31137812-C-A

39065669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31137812-C-G

39065669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31137812-C-T

39065684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31137827-G-A

39065684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31137827-G-T

http://identifiers.org/hco/6/GRCh38#39065705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31137848-C-A

39065705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 31137848-C-T

39065849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31137989-T-C

39065852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31137992-G-A

39065852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31137992-G-T

http://identifiers.org/hco/6/GRCh38#39065883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31138019-C-A

39065883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31138019-C-T

39065893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31138029-G-A

39065893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31138029-G-T

39065910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31138046-T-C

http://identifiers.org/hco/6/GRCh38#39065919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31138055-C-A

39065974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31138109-T-C

http://identifiers.org/hco/6/GRCh38#39066043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31138169-C-A

39066043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31138169-C-T

39066149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31138262-G-A

39066149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31138262-G-T

39066157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31138283-T-C

http://identifiers.org/hco/6/GRCh38#39066165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31138294-C-A

39066165-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31138294-C-G

39066168-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31138297-T-A

39066168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31138297-T-C

39066168-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31138297-T-G

39066241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31138374-G-A

39066241-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31138374-G-C

39066317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31138451-G-A

39066317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31138451-G-T

http://identifiers.org/hco/6/GRCh38#39066320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31138454-C-A

39066320-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31138454-C-G

39066320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31138454-C-T

39066323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31138457-G-A

39066328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31138465-G-A

39066328-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31138465-G-C

39066328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31138465-G-T

39066344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31138481-A-G

39066344-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31138481-A-T

http://identifiers.org/hco/6/GRCh38#39066345-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31138482-A-C

39066345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31138482-A-G

39066382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31138505-A-G

39066680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31138957-G-A

http://identifiers.org/hco/6/GRCh38#39066706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31138982-C-A

39066747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31139024-T-C

39066750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31139027-A-G

39066938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31139251-C-T

http://identifiers.org/hco/6/GRCh38#39072522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31143153-C-A

39072541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31143171-T-C

http://identifiers.org/hco/6/GRCh38#39072745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31143345-C-A

39072745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31143345-C-T

39072841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31143454-A-G

39073029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31143642-C-T

39073034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31143647-A-G

39073034-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31143647-A-T

39073116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31143941-G-A

39073116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31143941-G-C

39073116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31143941-G-T

39073126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31143951-G-A

39073126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31143951-G-T

39073156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31143997-G-A

39073442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31144327-A-G

39073522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31144405-G-A

39073522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31144405-G-C

39073678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31144560-C-G

39073678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31144560-C-T

http://identifiers.org/hco/6/GRCh38#39073690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31144572-C-A

39073690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31144572-C-T

39073823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31144717-G-A

39073823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31144717-G-T

http://identifiers.org/hco/6/GRCh38#39074175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31145125-C-A

39074175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31145125-C-G

39074175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31145125-C-T

http://identifiers.org/hco/6/GRCh38#39074212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31145151-C-A

39074212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31145151-C-T

39074230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31145169-A-G

39074272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31145199-G-A

39074272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31145199-G-T

http://identifiers.org/hco/6/GRCh38#39074307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31145234-C-A

39074307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31145234-C-T

39074365-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31145291-T-G

39074435-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31145349-T-G

39075565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31145993-C-T

39075718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31146108-A-G

39076109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31146259-A-G

39076650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31147168-G-A

http://identifiers.org/hco/6/GRCh38#39076992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31147474-C-A

39076992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31147474-C-T

39077125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31147596-G-A

39077125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31147596-G-T

39077787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31148435-G-A

39077809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31148449-T-C

39077862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31148489-G-T

http://identifiers.org/hco/6/GRCh38#39078172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31148769-C-A

39078172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31148769-C-T

http://identifiers.org/hco/6/GRCh38#39078191-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31148777-A-C

39078240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31148826-G-T

39078263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31148850-G-A

39078263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31148850-G-T

39078292-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31148879-T-G

39078309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31148897-C-G

39078309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31148897-C-T

39078389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 31148982-G-A

39078389-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 31148982-G-C

http://identifiers.org/hco/6/GRCh38#39078529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31149125-C-A

39078529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31149125-C-T

39078598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31149175-G-A

39078789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31149356-A-G

39078830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31149387-G-T

39078834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31149391-C-T

http://identifiers.org/hco/6/GRCh38#39078854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31149399-C-A

39078854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31149399-C-T

39078869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31149414-T-C

39078869-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31149414-T-G

http://identifiers.org/hco/6/GRCh38#39078920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31149463-C-A

39078920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31149463-C-T

39079053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31149598-T-C

39079085-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31149659-C-G

39079085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31149659-C-T

39079098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31149670-G-T

39079108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 31149688-G-A

39079144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31149724-C-T

39079147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31149727-C-T

http://identifiers.org/hco/6/GRCh38#39079255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31149823-C-A

39079255-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31149823-C-G

39079255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31149823-C-T

39079256-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31149824-T-A

39079256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31149824-T-C

39079256-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31149824-T-G

39079257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31149825-A-G

39079257-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31149825-A-T

39079286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31149846-G-T

http://identifiers.org/hco/6/GRCh38#39079324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31149883-C-A

39079324-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31149883-C-G

39079417-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31149981-A-T

39079491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31150047-G-A

39079491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31150047-G-C

39079528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31150087-T-C

39079681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31150240-G-A

http://identifiers.org/hco/6/GRCh38#39079696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31150255-C-A

39079696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31150255-C-T

39079759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31150317-A-G

http://identifiers.org/hco/6/GRCh38#39079763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31150321-C-A

39079763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31150321-C-T

39079782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31150340-G-A

39079782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31150340-G-T

http://identifiers.org/hco/6/GRCh38#39079823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31150364-C-A

39079823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31150364-C-T

http://identifiers.org/hco/6/GRCh38#39079827-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31150368-A-C

39079827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31150368-A-G

39079841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31150382-G-A

39079841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31150382-G-T

http://identifiers.org/hco/6/GRCh38#39079984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31150520-C-A

39080567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31151484-G-A

39080567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31151484-G-T

39080598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31151515-G-A

39080598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31151515-G-T

39080636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31151525-G-T

39080638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31151527-G-A

39083663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31152362-C-T

39083690-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31152382-A-T

39083765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31152650-G-A

39084122-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31153004-G-C

39084374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31153636-G-A

39084471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31153691-A-G

39084901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31154102-C-T

39084902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31154103-G-A

39084902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31154103-G-T

39085012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31154202-T-C

39085083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31154273-A-G

39085144-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31154317-G-C

39085224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31154405-T-C

39085356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31154554-C-T

39085517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31154847-G-A

39085659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31154983-G-A

39085928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31155261-G-A

39085959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31155292-C-T

39085962-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31155295-C-G

39085962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31155295-C-T

http://identifiers.org/hco/6/GRCh38#39086122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31155453-C-A

39086122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31155453-C-T

39086159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31155487-A-G

39086159-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31155487-A-T

http://identifiers.org/hco/6/GRCh38#39086182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31155525-C-A

39086182-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31155525-C-G

39086182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31155525-C-T

39086271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31155613-G-T

39086536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31155877-T-C

39086582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31155930-T-C

39086683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31156037-G-A

39086683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31156037-G-T

39086963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31156273-G-A

39086980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31156290-C-T

http://identifiers.org/hco/6/GRCh38#39087053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31156359-C-A

39087082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31156393-G-T

39087159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31156443-A-G

39087282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31156552-G-A

39087282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31156552-G-T

39087315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31156582-G-A

39087315-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31156582-G-C

39087315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31156582-G-T

http://identifiers.org/hco/6/GRCh38#39087345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31156615-C-A

39087347-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31156617-C-G

39087466-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31156740-A-T

39087524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31156802-G-A

39087524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31156802-G-T

39087535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31156813-C-T

39087595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31156872-A-G

39087602-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31156879-C-G

http://identifiers.org/hco/6/GRCh38#39087826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31157111-C-A

http://identifiers.org/hco/6/GRCh38#39087854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31157153-C-A

http://identifiers.org/hco/6/GRCh38#39087884-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#31157182-A-C

39087939-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31157219-T-G

39088296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31157490-G-A

39088357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 31157574-G-A

39088386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 31157603-C-T

http://identifiers.org/hco/6/GRCh38#39088546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#31157769-C-A

39088908-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31158130-G-C

39089393-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31158784-C-G

39089461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31158838-G-A

39089508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31158862-C-T

39089509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31158863-T-C

39089683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31158951-G-A

39089885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31159161-G-A

39090038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4324
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31159344-T-C