31064666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149468065-C-T

31064707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149468112-G-T

31064933-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149468161-G-C

31065005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: non coding transcript exon variant
orthologous variants: 149468234-G-A

http://identifiers.org/hco/13/GRCh38#31065008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149468237-C-A

31065008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: non coding transcript exon variant
orthologous variants: 149468237-C-T

http://identifiers.org/hco/13/GRCh38#31065063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149468292-C-A

31065444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149468378-C-T

31065803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149468672-T-C

31065850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149468720-G-A

31066905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149475497-C-T

31066906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149475498-G-A

31066924-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149475516-G-C

31067387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: non coding transcript exon variant
orthologous variants: 149475940-C-T

31067526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149476042-G-T

http://identifiers.org/hco/13/GRCh38#31067564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149476078-C-A

31067564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149476078-C-T

31067709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149476189-C-G

31067719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149476199-C-T

31069049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149478734-T-C

31069143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149478838-G-A

31069143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149478838-G-T

31070237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149479107-C-T

31070372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149479248-C-T

31070966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149479774-C-T

31073279-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149484061-T-A

31073427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149484190-G-A

31073567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149484343-T-C

31073628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149484403-G-T

31073773-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149484563-T-A

31073775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149484565-A-G

31073784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149484574-G-A

31073950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149484730-C-T

31074105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149484877-A-G

31074325-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149485106-T-G

31074663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149485345-T-C

31074671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149485352-C-T

31075235-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149485441-A-T

31075290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149485498-C-T

31076386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149486742-G-A

31076656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149487234-A-G

31076708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149487294-A-G

31076934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149487508-T-C

31076970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149487540-G-A

31077009-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149487580-C-G

31077050-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149487622-T-A

31077061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149487633-T-C

31077110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: non coding transcript exon variant
orthologous variants: 149487682-G-T

31077185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: non coding transcript exon variant
orthologous variants: 149487757-G-A

31077185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: non coding transcript exon variant
orthologous variants: 149487757-G-T

http://identifiers.org/hco/13/GRCh38#31077443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149488004-C-A

31077443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149488004-C-T

http://identifiers.org/hco/13/GRCh38#31077451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149488012-C-A

31077451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149488012-C-T

http://identifiers.org/hco/13/GRCh38#31078619-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149488862-A-C

31078619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149488862-A-G

http://identifiers.org/hco/13/GRCh38#31078713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149488933-C-A

31078713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149488933-C-T

31078716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149488936-G-A

31078716-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149488936-G-C

31078754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149488959-A-G

http://identifiers.org/hco/13/GRCh38#31078800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149488991-C-A

31078922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149489097-G-A

31079062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149489249-G-A

31079272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149489425-C-T

31079384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149489521-G-A

31079436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149489572-T-C

31079998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149490385-G-A

31080091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149490475-G-A

http://identifiers.org/hco/13/GRCh38#31080183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149490549-C-A

31080183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149490549-C-T

31080373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149490732-A-G

31083493-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149491176-A-T

31083547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149491229-G-A

31083559-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149491238-A-T

31083609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149491287-A-G

31083795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149491453-A-G

31083808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149491466-G-A

31083808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149491466-G-T

31084286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149491751-G-A

31084286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149491751-G-T

31084335-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149491800-T-A

31084381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149491847-A-G

31084441-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149491916-C-G

31084527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149492003-G-A

31084554-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149492033-G-C

31085048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149492582-T-C

31085121-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149492655-A-T

31085224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149492757-G-A

31085279-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149492812-C-G

31085778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149493780-A-G

31086018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149493940-G-C

31086458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149494174-G-A

31086520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149494236-T-C

31086570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149494277-C-T

31087394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149495573-G-A

31087419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149495602-C-T

31087454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149495636-G-A

31087641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149495829-A-G

31087769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149495963-T-C

31088059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149496148-C-T

31088080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149496167-C-T

31088438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149496696-G-T

31088643-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149496996-C-G

31088643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149496996-C-T

31088659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149497024-A-G

http://identifiers.org/hco/13/GRCh38#31088705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149497078-C-A

31088705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149497078-C-T

31088706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149497079-G-A

31088709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149497082-C-T

31088729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149497101-T-C

http://identifiers.org/hco/13/GRCh38#31088809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149497195-C-A

31088809-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149497195-C-G

31088809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149497195-C-T

31088835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149497221-A-G

31088876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149497224-G-A

http://identifiers.org/hco/13/GRCh38#31089155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149497374-C-A

31089155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149497374-C-T

31089232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149497447-T-C

31089274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149497489-G-T

31089275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 149497490-G-T

31089363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: non coding transcript exon variant
orthologous variants: 149497579-T-C

31089416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149497636-G-A

31089433-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149497653-G-C

31089481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149497699-T-C

31090700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149499954-G-A

31090700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149499954-G-T

31090814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149500037-T-C

31091033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149500462-G-T

31091402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149500807-T-C

31092305-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149501288-C-G

31092305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149501288-C-T

http://identifiers.org/hco/13/GRCh38#31092553-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149501511-A-C

31092553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149501511-A-G

31092553-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149501511-A-T

31092807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149502379-G-A

http://identifiers.org/hco/13/GRCh38#31092910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149502469-C-A

31092910-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149502469-C-G

http://identifiers.org/hco/13/GRCh38#31092928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149502484-C-A

http://identifiers.org/hco/13/GRCh38#31092977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149502532-C-A

31093006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: non coding transcript exon variant
orthologous variants: 149502561-C-T

31093021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: non coding transcript exon variant
orthologous variants: 149502576-G-T

31093083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149502638-G-A

31093224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149502760-T-C

31093228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149502764-G-C

31099095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 149505287-T-C

31099747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149506126-G-A

31099874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149506251-T-C

31100006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149506402-A-G

31100227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149506604-G-A

31100245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149506622-A-G

http://identifiers.org/hco/13/GRCh38#31101535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149507730-C-A

31101535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149507730-C-T

31101598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149507793-A-G

31101608-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149507803-A-T

31101618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149507811-G-A

31101618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149507811-G-T

31101707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149507902-C-T

31101936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149508127-C-T

31101952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149508138-C-T

31102362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149508465-A-G

31102634-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149508795-T-A

http://identifiers.org/hco/13/GRCh38#31102647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149508807-C-A

31102721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149508943-A-G

31102853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149509063-C-T

31102898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149509108-T-C

31102964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149509179-G-T

31103070-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149509281-A-T

http://identifiers.org/hco/13/GRCh38#31103103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149509305-C-A

http://identifiers.org/hco/13/GRCh38#31103141-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149509350-A-C

31103142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149509351-C-T

31103364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149509539-G-A

31103368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149509543-G-A

31103368-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149509543-G-C

31103631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149509729-G-A

31105022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: non coding transcript exon variant
orthologous variants: 149511559-C-T

http://identifiers.org/hco/13/GRCh38#31105113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149511677-C-A

http://identifiers.org/hco/13/GRCh38#31105219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149511762-C-A

31105219-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149511762-C-G

31105219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149511762-C-T

http://identifiers.org/hco/13/GRCh38#31105227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149511770-C-A

http://identifiers.org/hco/13/GRCh38#31105257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149511800-C-A

31105267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149511810-T-C

31105269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149511812-G-T

31105330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149511849-C-T

31105396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149511922-C-T

31105453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149511983-C-T

31105478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149512012-C-T

31105479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149512013-G-A

31105488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149512022-C-T

31105637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149512155-C-G

31105659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149512177-G-A

31105709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149512229-C-T

http://identifiers.org/hco/13/GRCh38#31105943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149512332-C-A

31105974-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149512363-A-T

31106146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149512492-G-A

31106146-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149512492-G-C

31106191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149512537-C-T

http://identifiers.org/hco/13/GRCh38#31106490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149512825-C-A

http://identifiers.org/hco/13/GRCh38#31106546-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149512882-A-C

31106585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149512920-T-C

31106591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149512926-A-G

31106593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149512928-G-A

31107144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149513201-C-T

31107339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149513503-C-T

31107356-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149513511-T-A

31107356-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149513511-T-G

31107463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149513595-C-T

31107473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149513605-G-A

31107572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149513697-G-A

31107642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149513756-G-A

31107800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149513902-C-T

31107813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149513915-A-G

31107911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149514001-C-T

31107926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149514016-G-A

31109666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149515281-C-T

31109758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149515383-T-C

31110222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149516425-C-T

31110238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149516441-G-A

31110267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149516502-G-A

31110321-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149516586-G-C

31110321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149516586-G-T

31110434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149516694-G-A

31110466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149516725-G-A

31110538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149516796-C-T

31110733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149517044-G-A

31110890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149517174-G-A

31111007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149517291-G-A

31111010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149517296-G-A

31111113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149517406-G-A

31111253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149517533-C-T

http://identifiers.org/hco/13/GRCh38#31111262-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149517539-A-C

31111758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: non coding transcript exon variant
orthologous variants: 149517949-C-T

31111788-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: non coding transcript exon variant
orthologous variants: 149517979-C-G

http://identifiers.org/hco/13/GRCh38#31112094-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149518739-A-C

http://identifiers.org/hco/13/GRCh38#31112099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149518744-C-A

31112099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: non coding transcript exon variant
orthologous variants: 149518744-C-T

31112124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: non coding transcript exon variant
orthologous variants: 149518769-T-C

http://identifiers.org/hco/13/GRCh38#31112126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149518771-C-A

31112126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: non coding transcript exon variant
orthologous variants: 149518771-C-T

31112217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149518862-C-T

31112386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149519031-G-A

31112446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149519087-G-A

31113643-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149519653-T-A

http://identifiers.org/hco/13/GRCh38#31113723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149519736-C-A

31113723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149519736-C-T

31113727-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149519740-A-T

31113737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149519750-C-T

31113743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149519756-G-C

31113743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149519756-G-T

31113837-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149519782-T-A

31113838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149519783-G-T

31114340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149520843-G-T

http://identifiers.org/hco/13/GRCh38#31114595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149521062-C-A

31114595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149521062-C-T

31114664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149521118-G-T

31114799-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149521239-G-C

31115199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149521616-G-T

31115321-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149522419-A-T

31115330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149522427-G-T

31115429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149522514-G-T