134600153-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102423244-A-T

http://identifiers.org/hco/3/GRCh38#134600678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102422758-C-A

134600678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102422758-C-T

134600828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102422593-G-T

134600877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102422514-A-G

134600903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102422481-A-G

134601020-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 102422397-G-C

134601020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 102422397-G-T

134601091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102422325-A-G

http://identifiers.org/hco/3/GRCh38#134601253-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102422162-A-C

134601253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102422162-A-G

http://identifiers.org/hco/3/GRCh38#134601254-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102422161-A-C

134601254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102422161-A-G

134601254-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102422161-A-T

http://identifiers.org/hco/3/GRCh38#134601310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102422104-C-A

134601310-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102422104-C-G

134601429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102421988-A-G

134601469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102421948-G-A

134601738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102421682-G-A

134602186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102421281-G-T

134602273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102421187-G-A

134602344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102421109-C-T

134602451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102420994-G-A

http://identifiers.org/hco/3/GRCh38#134602638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102420818-C-A

134602990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102420521-T-C

134602990-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102420521-T-G

134603085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102420442-G-A

134603085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102420442-G-T

http://identifiers.org/hco/3/GRCh38#134603100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102420427-C-A

134603100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102420427-C-T

http://identifiers.org/hco/3/GRCh38#134603244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102420311-C-A

134603244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102420311-C-T

http://identifiers.org/hco/3/GRCh38#134603313-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102420255-A-C

134603313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102420255-A-G

134603313-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102420255-A-T

http://identifiers.org/hco/3/GRCh38#134603384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102420184-C-A

134603384-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102420184-C-G

134603384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102420184-C-T

http://identifiers.org/hco/3/GRCh38#134603392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102420176-C-A

134603392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102420176-C-T

http://identifiers.org/hco/3/GRCh38#134603414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102420155-C-A

134603414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102420155-C-T

134603415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102420154-A-G

134603442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102420127-G-A

134603442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102420127-G-T

134603491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102420064-G-A

134603491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102420064-G-T

134603541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102420014-C-T

134603569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102419989-G-A

134603751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 102419806-G-A

134603751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 102419806-G-T

http://identifiers.org/hco/3/GRCh38#134603805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102419752-C-A

134603805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 102419752-C-G

134603805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 102419752-C-T

134603934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 102419623-T-C

134603973-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 102419584-C-G

134604069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 102419488-T-C

134604110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 102419447-G-A

134604150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 102419407-A-G

134604165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 102419392-G-A

134604210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 102419347-A-G

134604285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 102419272-G-A

134604471-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 102419086-T-G

134604488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102419069-G-A

134604555-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102419018-T-A

134604556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102419017-G-A

134604556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102419017-G-T

134604560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102419013-G-A

134604560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102419013-G-T

134604642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102418937-A-G

134604899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102418645-G-A

134604899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102418645-G-C

134604902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102418642-T-C

134605007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102418243-C-G

134605053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102418201-A-G

134605082-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102418179-G-C

134605239-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102418068-T-A

134605241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102418066-C-T

134605334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102417985-A-G

134605347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102417972-G-A

134605388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102417932-C-T

134606683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102417527-A-G

134606686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102417524-G-A

http://identifiers.org/hco/3/GRCh38#134606891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102417383-C-A

134606891-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102417383-C-G

134606899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102417375-T-C

134606920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102417351-T-C

134606945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102417326-C-T

134607120-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102417154-T-A

134607120-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102417154-T-G

134607155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102417119-T-C

134607202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102417074-G-T

134607277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102417010-G-A

134607316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102416973-G-T

134607350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102416930-G-A

http://identifiers.org/hco/3/GRCh38#134607362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102416915-C-A

134607365-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102416912-C-G

134607365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102416912-C-T

134607368-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102416909-T-A

134607368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102416909-T-C

134607412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102416852-T-C

134607412-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102416852-T-G

http://identifiers.org/hco/3/GRCh38#134607417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102416847-C-A

134607417-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102416847-C-G

134607417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102416847-C-T

http://identifiers.org/hco/3/GRCh38#134607432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102416835-C-A

134607471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102416796-G-A

http://identifiers.org/hco/3/GRCh38#134607537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102416729-C-A

134607537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102416729-C-T

http://identifiers.org/hco/3/GRCh38#134607610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102416666-C-A

134607610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102416666-C-T

http://identifiers.org/hco/3/GRCh38#134607621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102416655-C-A

134607621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102416655-C-T

134607628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102416648-G-A

134607628-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102416648-G-C

134607628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102416648-G-T

134607703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102416553-G-T

134607710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102416545-A-G

134607747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102416509-G-T

134608807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102416227-G-A

134608862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102416171-A-G

134608871-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102416162-C-G

134608871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102416162-C-T

134608874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102416143-C-T

134608876-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102416118-T-A

134608876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102416118-T-C

134608932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102416043-A-G

134608932-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102416043-A-T

http://identifiers.org/hco/3/GRCh38#134608946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102416033-C-A

134608979-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102416000-C-G

134608979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102416000-C-T

134609068-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102415914-A-T

134609491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102415554-A-G

134609662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102415385-C-T

134609778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102415307-A-G

134609804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102415296-G-A

http://identifiers.org/hco/3/GRCh38#134609908-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102415265-A-C

134609908-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102415265-A-T

134610048-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102415136-A-T

134610123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102415059-T-C

134610157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102415025-C-T

134610184-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102414997-C-G

134610184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102414997-C-T

http://identifiers.org/hco/3/GRCh38#134610185-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102414996-A-C

134610185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102414996-A-G

134610214-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102414967-T-G

134610282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102414899-G-A

134610558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102414750-T-C

http://identifiers.org/hco/3/GRCh38#134610699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102414617-C-A

134610699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102414617-C-T

http://identifiers.org/hco/3/GRCh38#134610781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102414536-C-A

134610781-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102414536-C-G

134610781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102414536-C-T

134610795-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102414522-T-G

http://identifiers.org/hco/3/GRCh38#134610797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102414520-C-A

134610797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102414520-C-T

134610800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102414517-G-T

134610833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102414485-G-A

134610838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102414480-T-C

134610893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102414472-G-T

134610979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102414397-G-A

134610979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102414397-G-T

134611069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102414314-T-C

134611891-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102413173-G-C

134611938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102413126-T-C

134612039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102413030-A-G

http://identifiers.org/hco/3/GRCh38#134612215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102412828-C-A

134612215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102412828-C-T

134612719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102412235-A-G

134612818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102412170-A-G

134612825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102412164-G-T

134612826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102412163-G-T

134612844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102412147-A-G

134612957-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102411935-A-T

http://identifiers.org/hco/3/GRCh38#134613025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102411883-C-A

134613025-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102411883-C-G

134613121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102411789-A-G

134613163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102411750-T-C

134613387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102411557-G-A

134613404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102411540-C-T

http://identifiers.org/hco/3/GRCh38#134613417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102411530-C-A

134613417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102411530-C-T

134613899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102411043-A-G

134613948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102410994-G-A

134613961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102410967-T-C

134614059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102410878-T-C

134614223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102410803-A-G

134614275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102410759-T-C

http://identifiers.org/hco/3/GRCh38#134614423-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102410607-A-C

134614423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102410607-A-G

134614423-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102410607-A-T

134614562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102410477-A-G

134615280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102409952-G-A

134615280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102409952-G-T

134615337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102409895-T-C

134615352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102409881-T-C

http://identifiers.org/hco/3/GRCh38#134615571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102409832-C-A

134615571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102409832-C-T

134615577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102409826-T-C

134616015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102409161-G-A

134616192-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102408982-T-A

134616192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102408982-T-C

134616604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102408551-A-G

134616869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102408285-G-A

134616922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102408239-A-G

134616922-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102408239-A-T

134617066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102408100-G-C

134617295-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102407382-A-T

134618089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102406160-G-T

134618116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102406142-C-T

134618585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102405732-C-T

134618782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102405596-G-A

134618810-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102405568-T-G

134619043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102405335-T-C

134619108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102405268-T-C

134619113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102405263-C-T

134619133-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102405243-T-G

134619256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102405106-A-G

134619277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102405085-G-A

134619277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102405085-G-T

134619370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102404970-A-G

http://identifiers.org/hco/3/GRCh38#134619394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102404946-C-A

134619394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102404946-C-T

http://identifiers.org/hco/3/GRCh38#134619488-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102404859-A-C

http://identifiers.org/hco/3/GRCh38#134619923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102404692-C-A

http://identifiers.org/hco/3/GRCh38#134619925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102404690-C-A

134619925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102404690-C-T

134619933-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102404682-C-G

134619961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102404664-G-A

134619961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102404664-G-T

134620075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102404569-C-T

134620080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102404564-T-C

134620096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102404550-C-T

134620274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102404389-G-A

134620278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102404385-A-G

134620307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102404349-G-T

http://identifiers.org/hco/3/GRCh38#134620386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102404286-C-A

134620393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102404279-G-A

134620406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102404267-G-A

134620415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102404258-C-T

134620476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102404200-A-G

http://identifiers.org/hco/3/GRCh38#134620523-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102404172-A-C

134620613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102404142-A-G

134620623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102404132-T-C

134620623-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102404132-T-G

134620727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102404023-G-T

134620743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102404007-G-C

134620743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102404007-G-T

134620799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102403951-G-A

134620863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 102403888-G-A

134620863-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 102403888-G-C

134620863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 102403888-G-T

134620888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102403863-G-A

134620902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102403855-G-A

134620902-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102403855-G-C

134620902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102403855-G-T

134621093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102403670-C-T

134624915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102402821-G-A

http://identifiers.org/hco/3/GRCh38#134624946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102402790-C-A

134624962-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102402774-T-G

134624978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102402758-G-T

http://identifiers.org/hco/3/GRCh38#134625024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102402706-C-A

134625024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102402706-C-T

134625057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102402673-G-A

134625057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 102402673-G-T

http://identifiers.org/hco/3/GRCh38#134625136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102402594-C-A

134625136-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 102402594-C-G

134625136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 102402594-C-T

134625154-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102402576-T-A

http://identifiers.org/hco/3/GRCh38#134625162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102402568-C-A

134625162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102402568-C-T

134626924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102401748-C-T

http://identifiers.org/hco/3/GRCh38#134626939-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102401734-A-C

134626964-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102401711-G-C

134627089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102401600-T-C

134627133-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102401549-T-A

134627295-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102401381-T-A

134627295-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102401381-T-G

134627398-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102401242-C-G

134627498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102400833-A-G

http://identifiers.org/hco/3/GRCh38#134627592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102400747-C-A

134627701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102400638-G-A

134627723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102400610-T-C

134627723-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102400610-T-G

134627847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102400492-G-A

134627847-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102400492-G-C

134627847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102400492-G-T

134627849-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102400490-T-A

134627865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 102400474-G-A

http://identifiers.org/hco/3/GRCh38#134627884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102400455-C-A

134627884-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102400455-C-G

134627884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102400455-C-T

134627910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102400433-G-T

134627927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102400416-C-T

http://identifiers.org/hco/3/GRCh38#134627955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102400387-C-A

134628131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 102400234-T-C

134628131-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 102400234-T-G

134628571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102399648-C-T

134628878-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102399483-T-G

134628982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102399406-C-T

134629012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102399382-G-T

134629111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102399294-T-C

134629143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102399262-A-G

134629422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102398984-A-G

134629442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102398964-G-T

http://identifiers.org/hco/3/GRCh38#134629615-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102398566-A-C

134629615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102398566-A-G

134629659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102398522-G-A

134629659-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102398522-G-C

134629659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102398522-G-T

134629838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102398344-A-G

134629838-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102398344-A-T

134629902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102398317-C-T

134630654-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102397570-T-A

134630727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102397505-G-A

134630760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102397474-T-C

http://identifiers.org/hco/3/GRCh38#134630957-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102397270-A-C

134631074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102397183-C-T

134631144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102397133-A-G

134631165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102397114-A-G

134636045-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102396369-T-G

134636052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102396362-A-G

134636087-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102396322-G-C

134636098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102396308-C-T

134636210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102396218-C-T

134636221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102396208-T-C

134636244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102396185-G-T

134636933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102395516-T-C

134637858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102394451-A-G

134638255-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102394141-G-C

134638256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102394140-A-G

134638952-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102393486-G-C

http://identifiers.org/hco/3/GRCh38#134639144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102393335-C-A

http://identifiers.org/hco/3/GRCh38#134640074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102393095-C-A

134640201-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102392989-T-A

134640201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102392989-T-C

134640317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102392888-C-T

134640360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102392833-G-A

134640367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102392826-G-T

134640415-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102392736-T-G

134640979-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102392178-C-G

134641021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102392135-G-A

134641021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102392135-G-T

134641075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102392078-G-A

134641075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102392078-G-T

134641117-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 102392043-G-C

134641125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102392036-T-C

134641151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102392009-T-C

134641176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102391966-A-G

134641376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102391721-T-C

134641413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102391687-A-G

http://identifiers.org/hco/3/GRCh38#134641563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102391538-C-A

134641787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102391371-C-T

134641982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102391229-G-A

http://identifiers.org/hco/3/GRCh38#134642317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102391166-A-C

134642423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102391087-A-G

134642448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102391069-C-T

http://identifiers.org/hco/3/GRCh38#134642670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102390834-C-A

134642734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102390773-G-A

134642784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102390728-G-A

http://identifiers.org/hco/3/GRCh38#134642806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102390706-C-A

134642806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102390706-C-T

134642935-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102390622-C-G

134642993-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102390579-T-G

134643223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102390323-T-C

134643237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102390309-C-T

134643246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102390302-T-C

http://identifiers.org/hco/3/GRCh38#134643267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102390281-C-A

134643276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102390272-C-G

http://identifiers.org/hco/3/GRCh38#134643277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102390271-C-A

134643473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102390061-G-A

134643473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102390061-G-T

134643474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102390060-G-T

134643623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102389945-G-T

134644301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102389585-C-T

134644391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102389507-C-T

http://identifiers.org/hco/3/GRCh38#134644458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102389437-C-A

134644716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102389215-C-T

134644810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102389109-A-G

134645573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102388353-A-G

134645621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102388311-A-G

134645679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102388035-C-G

134645966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102387790-C-T

134646007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102387751-G-T

134646102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102387664-G-A

134646129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102387637-T-C

134646192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102387580-G-C

http://identifiers.org/hco/3/GRCh38#134646527-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102387301-A-C

134646644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102387189-A-G

134646847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102387021-T-C

134646991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102386879-G-A

134647002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102386868-A-G

134647018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102386850-A-G

134647165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102386647-C-T

134647246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102386566-G-A

134647300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102386514-G-A

134647300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102386514-G-T

134647310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102386504-G-A

134647390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102386426-T-C

134647411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102386404-G-A

134647411-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102386404-G-C

134647411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102386404-G-T

134647537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102386259-G-A

134647537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102386259-G-T

134647544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102386246-A-G

http://identifiers.org/hco/3/GRCh38#134647599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102386193-C-A

134647599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102386193-C-T

134648073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102385775-G-A

134648106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102385742-G-A

134648573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102385509-G-A

134649139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102385026-C-T

134649252-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102384920-G-C

134649323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102384853-T-C

134649335-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102384841-C-G

134649729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102384481-C-T

134649738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102384472-C-T

134649746-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102384464-G-C

134649747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102384463-C-T

134650422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102383828-G-A

134650479-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102383766-C-G

134650689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102383624-C-T

http://identifiers.org/hco/3/GRCh38#134650755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#102383545-C-A

134650755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 102383545-C-T

http://identifiers.org/hco/3/GRCh38#134650765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#102383536-C-A

134650899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102383401-T-C

134650902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102383398-G-A

134651035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 102383265-G-A

134651035-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 102383265-G-C

134651035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 102383265-G-T

134651036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 102383264-C-T

134651083-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102383217-C-G

http://identifiers.org/hco/3/GRCh38#134651441-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#102382913-A-C

134651575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102382791-T-C

134651617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102382767-G-A

134651617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102382767-G-T