122865425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 124142788-G-T

122865447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 124142810-C-T

122865464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 124142827-G-A

122865464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 124142827-G-T

http://identifiers.org/hco/12/GRCh38#122865465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124142828-C-A

122865465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 124142828-C-T

122865485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 124142850-A-G

122865657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124142948-C-T

122865681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124142975-G-A

122865936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124143199-A-G

122865942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124143205-G-A

122865942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124143205-G-T

122865962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124143222-G-A

122865967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124143227-T-C

http://identifiers.org/hco/12/GRCh38#122866006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#124143254-C-A

122866006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124143254-C-T

122866030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124143268-T-C

122866048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124143286-T-C

122866054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124143292-A-G

122866057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124143295-G-A

122866092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124143329-T-C

122866099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124143336-G-T

122866129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124143381-G-T

122866259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124143506-C-T

122866575-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124143809-C-G

http://identifiers.org/hco/12/GRCh38#122866611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124143843-C-A

122866611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124143843-C-T

http://identifiers.org/hco/12/GRCh38#122866673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124143904-C-A

122866673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124143904-C-T

http://identifiers.org/hco/12/GRCh38#122866705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124143936-C-A

122866705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 124143936-C-T

122866735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 124143952-G-A

122866735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 124143952-G-T

http://identifiers.org/hco/12/GRCh38#122866816-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124144026-A-C

122866816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 124144026-A-G

http://identifiers.org/hco/12/GRCh38#122866821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124144031-C-A

122866821-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 124144031-C-G

122866821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 124144031-C-T

122866838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 124144048-A-G

http://identifiers.org/hco/12/GRCh38#122866887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124144094-C-A

122866888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 124144095-C-T

122866891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 124144098-T-C

122866891-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 124144098-T-G

122866972-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 124144167-T-A

122866972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 124144167-T-C

122867069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 3 prime UTR variant
orthologous variants: 124144262-C-T

122867106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 3 prime UTR variant
orthologous variants: 124144300-G-A

122867106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 3 prime UTR variant
orthologous variants: 124144300-G-T

122867111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 3 prime UTR variant
orthologous variants: 124144305-G-A

122867111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 3 prime UTR variant
orthologous variants: 124144305-G-T

122867146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: synonymous variant
orthologous variants: 124144340-A-G

122867146-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: synonymous variant
orthologous variants: 124144340-A-T

http://identifiers.org/hco/12/GRCh38#122867280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124144474-C-A

122867280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: missense variant
orthologous variants: 124144474-C-T

122867350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: synonymous variant
orthologous variants: 124144544-G-A

122867350-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: synonymous variant
orthologous variants: 124144544-G-C

122867350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: synonymous variant
orthologous variants: 124144544-G-T

122867449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: synonymous variant
orthologous variants: 124144643-C-T

122867640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron variant
orthologous variants: 124144837-G-A

122867640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron variant
orthologous variants: 124144837-G-T

http://identifiers.org/hco/12/GRCh38#122867726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124144924-C-A

122868182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron variant
orthologous variants: 124145384-T-C

http://identifiers.org/hco/12/GRCh38#122868366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124145547-C-A

122868366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron variant
orthologous variants: 124145547-C-T

122868369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron variant
orthologous variants: 124145550-G-T

122868399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron variant
orthologous variants: 124145581-G-A

122868399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron variant
orthologous variants: 124145581-G-T

122868510-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: synonymous variant
orthologous variants: 124145702-T-G

122868522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: synonymous variant
orthologous variants: 124145714-T-C

122868601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron variant
orthologous variants: 124145792-G-T

122868611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron variant
orthologous variants: 124145793-A-G

122868612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron variant
orthologous variants: 124145794-G-A

122868612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron variant
orthologous variants: 124145794-G-T

http://identifiers.org/hco/12/GRCh38#122868628-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124145810-A-C

122868641-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron variant
orthologous variants: 124145819-T-G

http://identifiers.org/hco/12/GRCh38#122868643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124145821-C-A

122868643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron variant
orthologous variants: 124145821-C-T

122868661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron variant
orthologous variants: 124145834-G-A

122868661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron variant
orthologous variants: 124145834-G-T

122870165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124148422-G-A

122870165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124148422-G-T

122870885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124148746-G-A

122870885-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124148746-G-C

122871016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 124148877-G-A

122871125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124148999-C-T

122871181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124149044-T-C

122871202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124149064-T-C

122871254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124149117-G-A

122871254-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124149117-G-C

122871267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124149130-A-G

122871272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124149135-G-A

122871272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124149135-G-T

122871379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124149220-G-A

122871379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124149220-G-T

122871477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 124149314-G-A

122871600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 124149430-T-C

122871600-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 124149430-T-G

122871624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 124149467-T-C

122871649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 124149475-G-A

122871649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 124149475-G-T

122871681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124149503-G-A

122871681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124149503-G-T

122871742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124149549-T-C

122871791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124149583-G-A

122871802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124149594-T-C

122871811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124149603-A-G

122871941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124149716-A-G

122871954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124149725-A-G

http://identifiers.org/hco/12/GRCh38#122871985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124149749-C-A

122871985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_donor_variant
orthologous variants: 124149749-C-T

122871991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 124149755-G-A

122871991-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 124149755-G-C

122871991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 124149755-G-T

http://identifiers.org/hco/12/GRCh38#122872094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124149857-C-A

122872094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124149857-C-T

122872147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124149895-G-A

122872147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124149895-G-T

122872156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124149905-C-T

122872162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124149911-T-C

122872172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124149920-T-C

122872173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124149921-G-A

122872173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124149921-G-T

122872230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124149958-G-A

122872230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124149958-G-T

122872231-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124149959-G-C

122872275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124149981-T-C

122872385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124150047-T-C

http://identifiers.org/hco/12/GRCh38#122872719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124150402-C-A

122872734-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124150412-C-G

http://identifiers.org/hco/12/GRCh38#122872749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124150427-C-A

122872749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124150427-C-T

122872814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124150488-A-G

http://identifiers.org/hco/12/GRCh38#122872861-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124150536-A-C

122872914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124150584-C-T

122872915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124150585-A-G

http://identifiers.org/hco/12/GRCh38#122872930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124150600-C-A

122872930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124150600-C-T

122872998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124150828-A-G

http://identifiers.org/hco/12/GRCh38#122873014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124150844-C-A

122873014-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124150844-C-G

122873099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124150913-G-A

122873099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124150913-G-T

122873110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124150924-G-T

http://identifiers.org/hco/12/GRCh38#122873131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124150945-C-A

122873131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124150945-C-T

122873146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124150963-A-G

http://identifiers.org/hco/12/GRCh38#122874317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#124152380-C-A

122874326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 124152389-C-T

122874352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124152416-G-A

122874352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124152416-G-T

122874370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124152434-G-A

http://identifiers.org/hco/12/GRCh38#122874371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124152435-C-A

http://identifiers.org/hco/12/GRCh38#122874418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124152485-C-A

122875004-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124152703-T-A

122875004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124152703-T-C

122875004-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124152703-T-G

http://identifiers.org/hco/12/GRCh38#122875007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124152706-C-A

122875007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124152706-C-G

122875896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124153022-G-T

http://identifiers.org/hco/12/GRCh38#122875946-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124153073-A-C

122876085-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124153215-T-A

122876085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124153215-T-C

http://identifiers.org/hco/12/GRCh38#122876181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124153314-C-A

122876181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124153314-C-T

http://identifiers.org/hco/12/GRCh38#122876196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124153329-C-A

http://identifiers.org/hco/12/GRCh38#122876227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124153363-C-A

122876403-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124153507-G-C

122876403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124153507-G-T

122876460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124153549-A-G

122876570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124153696-G-A

122876570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124153696-G-T

http://identifiers.org/hco/12/GRCh38#122876571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124153697-C-A

122876571-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124153697-C-G

122876593-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124153719-T-A

122876662-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124153774-A-T

122876683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124153799-G-A

122876683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124153799-G-T

http://identifiers.org/hco/12/GRCh38#122882876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124157367-C-A

122883032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124157523-T-C

http://identifiers.org/hco/12/GRCh38#122883135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124157625-C-A

122883885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124158205-C-T

122883946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124158261-G-A

122884001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124158315-C-T

122884117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124158480-A-G

122884142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124158495-A-G

122884158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124158511-C-T

http://identifiers.org/hco/12/GRCh38#122884739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124160418-C-A

122884739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124160418-C-T

122884754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124160432-T-C

http://identifiers.org/hco/12/GRCh38#122884990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124160620-C-A

122884993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124160622-G-T

122885195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124160813-C-G

122885228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124160846-A-G

122887175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124162694-G-A

122887234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124162743-T-C

http://identifiers.org/hco/12/GRCh38#122887239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124162748-C-A

122887301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124162812-G-A

122887301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124162812-G-T

122887573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124163077-A-G

http://identifiers.org/hco/12/GRCh38#122887576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124163080-C-A

122887576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124163080-C-T

122887592-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124163093-T-G

122887729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124163331-T-C

122887847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124163423-T-C

122887903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124163459-A-G

122887908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124163464-G-A

122887908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124163464-G-T

122887913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124163465-G-T

122887921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124163473-T-C

122887985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124163557-T-C

122888005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124163581-T-C

122888059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124163623-G-T

122888154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124163727-A-G

122888561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 124164136-T-C

122888643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124164205-T-C

http://identifiers.org/hco/12/GRCh38#122888648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124164210-C-A

122888679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 124164234-G-A

122888771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 124164351-A-G

http://identifiers.org/hco/12/GRCh38#122888926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124164495-C-A

http://identifiers.org/hco/12/GRCh38#122888966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124164523-C-A

http://identifiers.org/hco/12/GRCh38#122888982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124164532-C-A

122888982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 124164532-C-T

http://identifiers.org/hco/12/GRCh38#122889035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124164577-C-A

122889035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 124164577-C-T

122889056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 124164593-A-G

122889088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 124164624-G-T

122889100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 124164635-G-A

http://identifiers.org/hco/12/GRCh38#122889123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124164656-C-A

122889153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 124164676-G-A

122889168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 124164691-G-T

122889214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 124164741-A-G

122891766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron variant
orthologous variants: 124165682-T-C

122891776-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron variant
orthologous variants: 124165692-T-G

122892309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron variant
orthologous variants: 124166735-T-C

122892309-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron variant
orthologous variants: 124166735-T-G

122893214-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron variant
orthologous variants: 124167617-T-A

122893411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron variant
orthologous variants: 124167819-T-C

122893438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron variant
orthologous variants: 124167851-T-C

122893449-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron variant
orthologous variants: 124167865-T-A

122893533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron variant
orthologous variants: 124167940-T-C

http://identifiers.org/hco/12/GRCh38#122893813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124168191-C-A

122893852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron variant
orthologous variants: 124168246-G-A

122893852-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron variant
orthologous variants: 124168246-G-C

122893852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron variant
orthologous variants: 124168246-G-T

http://identifiers.org/hco/12/GRCh38#122893871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124168265-C-A

http://identifiers.org/hco/12/GRCh38#122893924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124168423-C-A

122894022-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron variant
orthologous variants: 124168567-C-G

122894189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron variant
orthologous variants: 124168732-G-A

122894213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron variant
orthologous variants: 124168760-T-C

122894293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron variant
orthologous variants: 124168852-C-T

122894569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron variant
orthologous variants: 124169162-T-C

122894605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron variant
orthologous variants: 124169196-G-A

122894842-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron_variant, undefined
orthologous variants: 124169403-G-C

122894866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: intron variant
orthologous variants: 124169431-G-A

122895985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: synonymous variant
orthologous variants: 124170198-G-A

122895985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: synonymous variant
orthologous variants: 124170198-G-C

122895985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: synonymous variant
orthologous variants: 124170198-G-T

122896006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: synonymous variant
orthologous variants: 124170219-G-A

122896006-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: missense variant
orthologous variants: 124170219-G-C

122896006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: missense variant
orthologous variants: 124170219-G-T

122896074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 124170286-G-A

122896074-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 124170286-G-C

122896074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 124170286-G-T

122896078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5 prime UTR variant
orthologous variants: 124170290-G-A

http://identifiers.org/hco/12/GRCh38#122896083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124170295-C-A

122896083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5 prime UTR variant
orthologous variants: 124170295-C-T

122896093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5 prime UTR variant
orthologous variants: 124170305-G-A

122896093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5 prime UTR variant
orthologous variants: 124170305-G-T

122896097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25754
most severe consequence: 5 prime UTR variant
orthologous variants: 124170312-C-T