126425189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133867677-T-C

http://identifiers.org/hco/10/GRCh38#126425272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133867742-C-A

126425310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 133867784-G-A

126425310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 133867784-G-T

126425325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133867797-G-A

126425325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133867797-G-T

126425335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133867807-C-T

126425365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133867837-G-T

126425394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133867858-A-G

126425492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133867934-G-A

http://identifiers.org/hco/10/GRCh38#126425502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133867956-C-A

126425502-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133867956-C-G

126425663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133868144-T-C

http://identifiers.org/hco/10/GRCh38#126425812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133868297-C-A

126425812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133868297-C-T

126425983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 133868458-G-A

126425983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 133868458-G-T

126426017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133868493-T-C

126426541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133869305-G-A

126426541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133869305-G-T

126426641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133869451-C-T

http://identifiers.org/hco/10/GRCh38#126426691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133869503-C-A

126426798-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133869609-T-A

126426942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133869725-C-T

126426978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133869761-T-C

http://identifiers.org/hco/10/GRCh38#126427060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133869851-C-A

126427224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133870015-C-T

126427276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133870065-T-C

126427311-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133870084-G-C

126427362-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133870133-T-G

126428106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133870288-G-A

126428129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133870313-G-A

126428130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133870314-C-T

126428138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133870322-C-T

126428203-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133870391-A-T

126428219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133870405-G-A

126428285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133870443-G-A

126428285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133870443-G-T

126428292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133870452-G-A

126429062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133871197-T-C

126429185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133871321-A-G

126429297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133871429-G-A

126429609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133871747-A-G

126429717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133871853-G-A

126429717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133871853-G-T

http://identifiers.org/hco/10/GRCh38#126429773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133871909-C-A

126429861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133871997-T-C

126429877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133872013-T-C

126429957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133872098-G-A

126429957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133872098-G-T

126429966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133872107-T-C

126429966-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133872107-T-G

126430224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133873039-A-G

126430404-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133873183-T-A

126430438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133873215-G-A

126430966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133873960-T-C

126431545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133874286-C-T

126431594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133874336-G-A

http://identifiers.org/hco/10/GRCh38#126431603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133874345-C-A

126431603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133874345-C-T

126431648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133874390-G-T

126431687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133874437-G-A

126431687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133874437-G-T

126431893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133874634-C-T

126433914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133876434-T-C

126434072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133876566-C-T

126434167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133876660-T-C

126434174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133876667-G-A

126434199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133876692-T-C

126434342-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133876838-T-A

126434612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133877076-C-T

126434631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133877094-T-C

126434737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133877210-C-T

126434753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133877226-G-A

126434790-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133877249-T-A

126434816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133877275-G-A

126435058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 133877513-C-T

126435079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133877533-C-T

126435137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133877594-G-A

http://identifiers.org/hco/10/GRCh38#126435232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133877673-C-A

126435356-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133877768-C-G

126435404-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133877811-T-G

126435471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133877863-A-G

126435499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133877878-C-T

http://identifiers.org/hco/10/GRCh38#126435528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133877907-C-A

126435549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133877922-C-T

126435755-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133878056-C-G

126435784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133878085-G-T

126435819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133878120-C-T

126435871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133878166-G-A

http://identifiers.org/hco/10/GRCh38#126436156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133878448-C-A

126436156-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133878448-C-G

126436287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133878540-A-G

126436325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133878581-G-A

126436470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133878715-C-T

126436488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133878733-G-C

126436488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133878733-G-T

126437781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133879244-C-T

126437785-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133879248-C-G

126437813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133879266-G-C

126438071-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133879465-C-G

126438186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133879555-C-T

126438212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133879583-C-T

126438283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133879651-T-C

126438287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133879655-A-G

126438425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133879802-G-A

126438509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133879894-G-A

126438568-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133879952-C-G

126438603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133879985-G-A

126438603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133879985-G-T

126451900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133888666-T-C

126451917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133888683-G-A

126452011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133888776-A-G

126452012-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133888777-T-A

126452567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133889291-A-G

126452671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133889395-A-G

126452674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133889398-G-T

126453257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133889986-G-T

126453264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133889993-C-T

126453616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133890259-C-T

126453624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133890266-G-T

126453633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133890275-C-T

126453693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133890333-G-T

126453932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133890501-T-C

126455839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133891565-A-G

126456314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133892040-A-G

126456347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133892073-T-C

126456347-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133892073-T-G

126456394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133892119-C-G

126456394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133892119-C-T

126456478-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133892205-C-G

126456478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133892205-C-T

126456563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133892291-T-C

126456564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133892292-G-A

126456800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133892537-G-A

126456867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133892607-C-T

126456876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133892616-C-T

http://identifiers.org/hco/10/GRCh38#126457823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133893510-C-A

126457823-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133893510-C-G

126457830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133893517-T-C

http://identifiers.org/hco/10/GRCh38#126457865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133893552-C-A

126457865-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133893552-C-G

126457865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133893552-C-T

126457879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133893566-T-C

126457922-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133893607-C-G

126458175-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133893862-G-C

126458205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133893892-A-G

126458314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133894001-G-A

126458442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133894126-G-T

126458562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 133894507-T-C

126458688-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 133894632-G-C

126458813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 133894757-T-C

126458932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133894850-G-A

126458932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133894850-G-T

http://identifiers.org/hco/10/GRCh38#126459021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#133894938-C-A

126459021-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 133894938-C-G

126459021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 133894938-C-T

126459024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 133894941-G-A

http://identifiers.org/hco/10/GRCh38#126459032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133894949-C-A

126459279-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133895198-T-A

126459298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133895219-G-A

126459298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133895219-G-T

126459304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133895225-G-A

126459304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133895225-G-T

126459345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133895266-G-T

126459346-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133895267-T-A

126459346-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133895267-T-G

http://identifiers.org/hco/10/GRCh38#126459352-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133895269-A-C

126459358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133895275-T-C

126459696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 133895621-G-A

126459701-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 133895626-A-T

http://identifiers.org/hco/10/GRCh38#126459761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133895672-C-A

126460967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133896276-C-T

126461347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133896634-T-C

126461393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 133896686-G-A

126461703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133897046-T-C

126462139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133897468-A-G

126462264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133897605-C-T

126462691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133897961-G-A

http://identifiers.org/hco/10/GRCh38#126462726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133897996-C-A

126462758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133898018-C-T

126462933-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133898151-C-G

126462933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133898151-C-T

http://identifiers.org/hco/10/GRCh38#126462972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133898187-C-A

126462972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133898187-C-T

126463074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133898295-T-C

http://identifiers.org/hco/10/GRCh38#126463097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133898318-C-A

126463097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133898318-C-T

126463159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133898380-A-G

126463159-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133898380-A-T

126463237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133898451-T-C

126463304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133898514-T-C

126463322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133898525-T-C

http://identifiers.org/hco/10/GRCh38#126463342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133898542-C-A

126463342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133898542-C-T

126463389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133898587-G-A

126463389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133898587-G-T

126463398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133898596-G-C

126463398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133898596-G-T

126463485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133898675-A-G

126463509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133898693-G-A

126463509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133898693-G-T

http://identifiers.org/hco/10/GRCh38#126463550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133898732-C-A

126463550-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133898732-C-G

126463650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133898855-C-T

126463702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133898913-G-A

http://identifiers.org/hco/10/GRCh38#126463778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133898976-C-A

126463779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133898977-A-G

126463830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133899024-G-A

126463938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133899115-T-C

126464185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133899366-C-T

126464242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133899425-C-T

126464304-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133899484-T-G

126464404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133899569-C-T

126464597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133899752-G-A

126464597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133899752-G-T

126464618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133899768-G-A

126464618-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133899768-G-C

126464618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133899768-G-T

126464651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133899801-G-A

126464651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133899801-G-C

126464651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133899801-G-T

126464687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133899836-G-A

126464688-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 133899837-C-G

126464815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 133899964-C-T

126464886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 133900035-G-A

126464886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 133900035-G-T

126464891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 133900040-G-A

http://identifiers.org/hco/10/GRCh38#126464999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133900145-C-A

126464999-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133900145-C-G

126464999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133900145-C-T

http://identifiers.org/hco/10/GRCh38#126465052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133900183-C-A

126465052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133900183-C-T

http://identifiers.org/hco/10/GRCh38#126465053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133900184-C-A

126465053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133900184-C-T

http://identifiers.org/hco/10/GRCh38#126465124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133900746-C-A

126465124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133900746-C-G

126465124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133900746-C-T

126465126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133900748-G-A

126465126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133900748-G-T

126465432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133901057-G-A

126465658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133901258-C-T

126466074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133901584-G-A

126466088-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133901596-T-A

http://identifiers.org/hco/10/GRCh38#126466199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133901697-C-A

126466199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133901697-C-T

126466524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133901873-C-T

126466779-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133902115-T-A

126466885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133902202-C-T

126466903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133902224-A-G

126467081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133902408-T-C

126467133-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133902455-T-G

126467150-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133902472-T-G

126467662-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133903458-A-T

126467792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133903585-T-C

126468430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133903823-G-A

126469061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133904356-A-G

126469201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133904493-A-G

126469257-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133904549-G-C

126470234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133904752-T-C

http://identifiers.org/hco/10/GRCh38#126470282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133904786-C-A

126470283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133904787-A-G

126470283-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133904787-A-T

126470772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133904871-G-A

http://identifiers.org/hco/10/GRCh38#126470810-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133904919-A-C

126470810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133904919-A-G

126470887-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133904997-G-C

126470966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133905072-C-T

126471045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133905152-G-A

126471099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133905214-C-T

126471106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133905221-C-T

126471144-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133905262-A-T

126471303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133905660-C-T

126471352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133905714-T-C

126471617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133906533-G-A

126471849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133906708-G-A

126471895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133906753-G-A

126471895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133906753-G-T

126472166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133907019-T-C

126474131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133908845-A-G

126474161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133908875-G-A

126474259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133908957-G-A

126474259-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133908957-G-C

126474263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133908961-G-A

126474324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133909016-G-A

126474429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133909126-A-G

126474524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133909221-T-C

126474582-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133909274-T-G

126474702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133909401-G-A

126474786-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133909487-A-T

126474812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133909513-A-G

http://identifiers.org/hco/10/GRCh38#126474816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133909517-C-A

126474816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133909517-C-T

126474881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133909579-G-A

126475042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133909721-C-T

126475154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133909838-T-C

http://identifiers.org/hco/10/GRCh38#126475214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133909904-C-A

126475223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133909914-A-G

126475223-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133909914-A-T

126475314-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133909989-C-G

126475324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133909998-C-T

126475576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133910239-T-C

126475695-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133910358-T-G

126475891-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133910552-T-A

126475969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133910598-G-A

http://identifiers.org/hco/10/GRCh38#126476007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133910645-C-A

http://identifiers.org/hco/10/GRCh38#126476338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133910872-C-A

http://identifiers.org/hco/10/GRCh38#126476455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133910988-C-A

126476529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 133911022-G-T

126476584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133911077-T-C

126476655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133911141-T-C

126476816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133911302-C-T

126476851-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133911325-C-G

126476851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133911325-C-T

126477184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133911805-G-A

126477199-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133911820-T-G

126477328-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133911968-T-A

126477657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133912300-T-C

126477708-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133912357-T-A

126477745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133912394-A-G

126477752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133912403-T-C

126478894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133913447-T-C

126479464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133913976-C-T

126479618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133914120-C-T

126479678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133914179-C-T

126479956-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133914730-G-C

126480072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133914857-C-T

126480124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133914910-A-G

126480557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133916478-G-T

http://identifiers.org/hco/10/GRCh38#126480586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133916507-C-A

126480586-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133916507-C-G

126480586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133916507-C-T

http://identifiers.org/hco/10/GRCh38#126480593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133916514-C-A

http://identifiers.org/hco/10/GRCh38#126482567-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133921661-A-C

126482592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133921686-C-T

126482710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133921810-G-A

http://identifiers.org/hco/10/GRCh38#126482754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133921856-C-A

126483189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133922809-A-G

http://identifiers.org/hco/10/GRCh38#126483686-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133923245-A-C

126483789-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133923349-A-T

126483814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133923375-C-T

126483815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133923376-A-G

126483854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133923419-G-A

126483961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133923480-C-T

126484122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133923572-A-G

126484215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133923667-C-T

126484220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133923672-A-G

126484352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133923791-A-G

126484742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133924115-G-A

126484828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133924206-G-A

126491394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133937538-G-A

http://identifiers.org/hco/10/GRCh38#126491490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133937610-C-A

126491490-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133937610-C-G

126491490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133937610-C-T

126491841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133937929-A-G

126491958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133938039-T-C

126492081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133938175-A-G

126492459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133938534-G-A

126492460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133938535-G-A

126492460-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133938535-G-C

126492522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133938594-T-C

126492830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133938752-T-C

126492982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133938888-C-T

126492991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133938897-T-C

126493300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133940751-G-A

126493354-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133940787-A-T

126493358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133940791-G-T

http://identifiers.org/hco/10/GRCh38#126493517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133940938-C-A

126493517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133940938-C-T

126493733-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133941020-A-T

http://identifiers.org/hco/10/GRCh38#126493982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133941229-C-A

126493982-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133941229-C-G

126494505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133941678-G-T

http://identifiers.org/hco/10/GRCh38#126494507-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133941680-A-C

126494578-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133941751-G-C

126494954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133942279-T-C

126494954-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133942279-T-G

126495520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133942534-G-A

126495613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133942627-G-A

http://identifiers.org/hco/10/GRCh38#126495747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133942759-C-A

126495747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133942759-C-T

126495902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133942910-A-G

126496143-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133943164-G-C

http://identifiers.org/hco/10/GRCh38#126496615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133943611-C-A

126496690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133943675-C-T

126496750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133943734-A-G

126496904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133943865-G-T

http://identifiers.org/hco/10/GRCh38#126496967-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133943925-A-C

126497042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133943983-G-A

126497265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133944214-G-A

126497296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133944245-G-A

126497296-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133944245-G-C

126497476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133944350-G-A

126497476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133944350-G-T

126497584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133944427-C-T

126497687-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133944512-T-G

126497926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133944729-C-T

126497960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133944761-G-A

126498419-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133945600-T-A

126498468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133945652-C-T

126498667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133945777-G-A

126498673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133945783-C-T

126498691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133945798-C-T

126498753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133945868-T-C

126498776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133945892-C-T

126498887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133945991-G-A

126498988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133946098-T-C

126499092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133946163-G-A

126499092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133946163-G-T

126499173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133946235-G-A

126499589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133946664-G-A

126499607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133946677-C-T

126499681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133946750-C-T

126499817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133947022-T-C

126499964-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133947164-T-A

126499965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133947165-G-A

126500073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133947269-A-G

126500119-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133947314-A-T

http://identifiers.org/hco/10/GRCh38#126500217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133947378-C-A

126500218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133947379-C-T

126500523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133947686-C-T

126500624-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133947763-C-G

126500717-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133947838-A-T

126500758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133947878-A-G

http://identifiers.org/hco/10/GRCh38#126501217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133948325-C-A

126502432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133949060-C-T

http://identifiers.org/hco/10/GRCh38#126502630-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133949180-A-C

126502630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133949180-A-G

http://identifiers.org/hco/10/GRCh38#126502702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133949233-C-A

126502702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133949233-C-T

126502813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133949342-T-C

126502862-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133949392-A-T

http://identifiers.org/hco/10/GRCh38#126502890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133949420-C-A

126502890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133949420-C-T

126502992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133949515-C-T

http://identifiers.org/hco/10/GRCh38#126503035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133949560-C-A

126503035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133949560-C-T

126503438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133949922-G-A

http://identifiers.org/hco/10/GRCh38#126503630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133950126-C-A

126503784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133950274-C-T

126503796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133950286-C-T

126503812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133950302-G-T

126503813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133950303-T-C

126503819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133950309-A-G

126503896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133950383-A-G

126503946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133950431-G-A

126503946-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133950431-G-C

126503946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133950431-G-T

126504031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 133950512-T-C

126504563-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 133951041-G-C

126504653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 133951131-C-T

126504656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 133951134-T-C

126504668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 133951146-G-A

126504795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 133951273-T-C

126504822-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 133951300-C-G

http://identifiers.org/hco/10/GRCh38#126504831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133951309-C-A

126504831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 133951309-C-T

126505036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 133951508-G-A

http://identifiers.org/hco/10/GRCh38#126505158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133951637-C-A

126505158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133951637-C-T

126505163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133951642-A-G

126505163-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133951642-A-T

126505165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133951644-G-A

126506186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133951719-T-C

126506222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133951753-T-C

126506329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133952240-A-G

http://identifiers.org/hco/10/GRCh38#126506527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133952368-C-A

126506748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133952558-G-T

126506777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133952590-G-T

http://identifiers.org/hco/10/GRCh38#126507434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133953063-C-A

126507517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133953129-G-A

126507567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133953152-T-C

126507681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133953252-G-A

126507681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133953252-G-T

http://identifiers.org/hco/10/GRCh38#126507791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133953349-C-A

126507835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133953386-C-T

126507994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133953547-G-T

http://identifiers.org/hco/10/GRCh38#126508053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133953605-C-A

126508053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133953605-C-T

126508150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133953701-T-C

126508537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133953857-C-T

126508772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133953949-G-A

126508772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133953949-G-C

126508772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133953949-G-T

126508857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133954028-C-T

126508859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133954030-T-C

126508862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133954033-G-A

126508879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133954049-G-A

126508971-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133954130-T-G

126509041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133954187-G-A

126509112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133954261-G-A

126509112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133954261-G-T

126509118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133954267-C-T

126509188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133954331-G-A

126509349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133954976-T-C

126509772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133955334-G-A

126510576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133955922-G-A

126510888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133956264-G-A

http://identifiers.org/hco/10/GRCh38#126510977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133956375-C-A

126511144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133956544-A-G

126511182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133956579-C-T

126511207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133956604-A-G

126511241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133956637-T-C

126511310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133956708-A-G

126511351-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133956749-T-A

126511368-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133956764-A-T

126511403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133956798-G-A

126511449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133956844-G-A

http://identifiers.org/hco/10/GRCh38#126511586-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133956970-A-C

126511586-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133956970-A-T

126511871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133957642-T-C

126511926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133957689-G-A

126511966-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133957712-T-G

http://identifiers.org/hco/10/GRCh38#126511978-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133957722-A-C

http://identifiers.org/hco/10/GRCh38#126512006-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133957730-A-C

126512010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133957734-G-T

126512016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 133957740-G-A

126512016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 133957740-G-T

126512104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133957816-A-G

126512125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133957837-T-C

http://identifiers.org/hco/10/GRCh38#126512154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133957869-C-A

126512163-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133957878-A-T

126512172-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133957888-A-T

126512390-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133957999-G-C

126512396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133958005-G-T

126512404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133958013-C-G

126512455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133958059-A-G

126512478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133958082-T-C

126512499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133958100-T-C

126512658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133958302-A-G

126512701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133958373-A-G

126513006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133958835-T-C

126513117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133958963-G-T

126513133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133958981-T-C

126513194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133959054-T-C

126513235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133959108-A-G

126513375-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133959249-T-A

126513424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133959296-C-T

126513508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133959380-C-T

126513577-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133959439-C-G

126513626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133959466-T-C

126513677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133959527-G-A

http://identifiers.org/hco/10/GRCh38#126513704-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133959579-A-C

126513827-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133959703-G-C

126513827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133959703-G-T

126513839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133959715-G-A

126513839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133959715-G-T

126513843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133959719-G-T

126513853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 133959729-T-C

126513909-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 133959785-T-A

126513950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133959826-G-T

126514064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133959944-A-G

126514064-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133959944-A-T

http://identifiers.org/hco/10/GRCh38#126514323-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133960577-A-C

126514341-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133960595-T-A

126514595-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133960746-C-G

126514764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133960921-A-G

126514952-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133961079-G-C

126515710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133961448-T-C

126515797-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133961538-C-G

126516221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133961944-G-T

126516539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 133962253-G-T

126516694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133962430-G-A

126516694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133962430-G-T

http://identifiers.org/hco/10/GRCh38#126516856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133962552-C-A

126517142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133962782-T-C

126517163-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133962803-T-G

126517194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133962838-G-T

126517242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133962885-G-A

126517317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133962964-A-G

126517332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133962976-A-G

126517366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133963011-G-A

126517376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133963021-G-A

126517402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133963046-C-T

126517970-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133963335-G-C

126518011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133963375-C-T

126518023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133963387-T-C

126518119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133963449-C-T

126518120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133963450-T-C

126518226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133963551-G-A

126518454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133963779-T-C

126518696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133963951-T-C

126518735-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133963988-C-G

126519037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133964187-C-T

126519756-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133965219-C-G

126519922-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133965395-C-G

http://identifiers.org/hco/10/GRCh38#126519980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133965458-C-A

126519980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133965458-C-T

126519988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133965463-T-C

126520013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133965488-G-A

126520111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133965532-G-A

126520139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133965564-A-G

http://identifiers.org/hco/10/GRCh38#126520267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133965680-C-A

126520267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133965680-C-T

126520270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133965683-G-T

126520319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133965735-A-G

126520394-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133965807-G-C

126520423-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133965835-T-A

126520429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133965841-A-G

http://identifiers.org/hco/10/GRCh38#126520451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133965863-C-A

126520451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133965863-C-T

126520458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133965870-G-T

126520459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133965871-G-A

126520459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133965871-G-T

http://identifiers.org/hco/10/GRCh38#126520460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133965872-C-A

126520460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133965872-C-T

http://identifiers.org/hco/10/GRCh38#126520488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133965931-C-A

126520488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133965931-C-T

126520558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 133965999-G-A

126520558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 133965999-G-T

http://identifiers.org/hco/10/GRCh38#126520879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133966096-C-A

126520879-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133966096-C-G

126520879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133966096-C-T

http://identifiers.org/hco/10/GRCh38#126520903-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133966121-A-C

126520903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133966121-A-G

126520903-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133966121-A-T

http://identifiers.org/hco/10/GRCh38#126520917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133966135-C-A

126520917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133966135-C-T

126520978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133966190-A-G

http://identifiers.org/hco/10/GRCh38#126520989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133966193-C-A

126520989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133966193-C-T

126521074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 133966271-G-A

http://identifiers.org/hco/10/GRCh38#126521082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#133966279-C-A

126521082-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 133966279-C-G

126521082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 133966279-C-T

126521209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133966378-G-T

126521215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133966385-A-G

126521243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133966413-C-T

126521498-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133966637-T-A

126521784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133967335-A-G

126521862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133967411-T-C

http://identifiers.org/hco/10/GRCh38#126523199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133968716-C-A

126523246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133968754-G-T

126523268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133968778-G-A

126523268-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133968778-G-C

126523298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133968805-C-T

126523329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133968845-G-A

126523329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133968845-G-T

126523333-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133968849-A-T

126523444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133968943-G-C

126523629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133969103-G-A

126523655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133969120-A-G

126523871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133969310-G-T

126523944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133969372-A-G

126524073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133969503-G-A

126524097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133969527-A-G

126524163-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133969794-G-C

126524163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133969794-G-T

126524284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133969974-G-A

126524314-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133970014-T-A

126524437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133970140-G-A

126524437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133970140-G-T

126524749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133970409-G-A

126524749-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133970409-G-C

126524749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133970409-G-T

126524760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 133970420-A-G

126524788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133970448-G-A

126524788-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133970448-G-C

http://identifiers.org/hco/10/GRCh38#126524848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133970519-C-A

126524914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133970593-C-T

126524928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133970607-T-C

126524942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133970621-T-C

126524942-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133970621-T-G

126525050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133970713-C-T

126525154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133970814-G-A

126525182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133970838-C-T

126525226-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133970881-G-C

126525276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133970929-C-G

http://identifiers.org/hco/10/GRCh38#126525286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133970939-C-A

126525286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133970939-C-T

126525412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133971026-G-A

126525436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133971050-G-A

126525740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133971368-A-G

126525967-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133971581-A-T

126526075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133971664-G-A

126526075-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133971664-G-C

126526201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133971781-C-T

126526680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133972349-A-G

126526725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133972395-G-A

126526745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133972415-T-C

126526820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133972487-T-C

126526821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133972488-G-A

126526825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133972492-G-A

126526881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133972531-A-G

126527312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133972931-T-C

126527476-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133973033-G-C

126527494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133973057-T-C

126527529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133973093-C-T

126527681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133973225-C-T

126527751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133973295-T-C

126527865-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133973408-T-A

126528285-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133973920-T-A

126528304-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133973931-C-G

126528305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133973932-A-G

126528603-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133974227-G-C

126528612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133974236-C-T

126528746-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133974369-T-G

126528748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133974371-G-T

126528852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133974663-G-A

126528924-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133974724-T-A

126528924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133974724-T-C

126528924-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133974724-T-G

126528947-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133974749-A-T

126529081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133974865-G-A

126529165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133974938-T-C

126529237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133975066-T-C

126529314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133975231-G-T

126529384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133975299-T-C

126529415-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133975338-T-A

126529422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133975345-A-G

126529574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133975482-G-A

126531588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133976110-G-T

126531599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133976121-C-T

http://identifiers.org/hco/10/GRCh38#126531775-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133976286-A-C

126531819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133976331-A-G

126531905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133976397-G-A

http://identifiers.org/hco/10/GRCh38#126532197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133976688-C-A

126532239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133976729-G-A

126532346-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133977243-T-G

126532353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133977250-C-T

126533285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133978159-T-C

126533342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133978209-C-T

126533749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133978561-G-A

126533920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133978732-G-A

126533992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133978803-A-G

http://identifiers.org/hco/10/GRCh38#126535751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133980084-C-A

126535751-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133980084-C-G

126535751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133980084-C-T

126535873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133980197-G-A

126535884-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133980204-C-G

126535884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133980204-C-T

126535890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133980210-C-T

126535946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133980266-G-A

http://identifiers.org/hco/10/GRCh38#126536577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133981061-C-A

126536729-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133981211-C-G

126536767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133981268-G-A

126537099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133981604-C-T

126537219-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133981712-T-A

126537503-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133981961-G-C

126537652-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133982108-T-G

126537765-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133982219-G-C

126537874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133982328-T-C

126537923-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133982381-C-G

126538241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133982765-C-T

126538719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133983200-G-A

126538954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133983418-C-T

126539146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133983593-C-T

126539759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133984163-A-G

126539771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133984175-T-C

126539848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133984249-G-A

126539975-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133984457-G-C

126539996-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133984494-T-G

http://identifiers.org/hco/10/GRCh38#126541195-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133985804-A-C

http://identifiers.org/hco/10/GRCh38#126541345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133985928-C-A

126541438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133986000-C-T

126541559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133986318-A-G

http://identifiers.org/hco/10/GRCh38#126541883-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133986623-A-C

http://identifiers.org/hco/10/GRCh38#126542002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133986737-C-A

126542010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133986745-C-G

126542016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133986751-A-G

126542053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133986794-G-C

126542084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133986824-G-A

126542101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133986841-A-G

126542114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133986854-G-A

126542193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133986917-G-A

126542354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133987659-T-C

http://identifiers.org/hco/10/GRCh38#126542502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133987797-C-A

126542502-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133987797-C-G

126542502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133987797-C-T

126543039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133988826-T-C

126543159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133988961-A-G

126543297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133989092-G-A

126543297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133989092-G-T

126543444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133989237-C-T

126543916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133989721-C-T

126544046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133989875-G-A

126544067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133990137-T-C

126544309-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133990356-T-G

126544318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133990365-C-T

126544437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133990441-G-A

126544455-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133990459-A-T

126544773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133990736-C-T

126544887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133990836-C-T

126545302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133991484-C-T

126545381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133991560-T-C

126545382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133991561-A-G

126545399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133991578-A-G

126545627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133991802-A-G

126551297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133996146-A-G

126554051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133997832-G-A

126554352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133998185-T-C

126554376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133998214-T-C

126554505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133998315-C-T

126554543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133998353-A-G

http://identifiers.org/hco/10/GRCh38#126554607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133998417-C-A

http://identifiers.org/hco/10/GRCh38#126554668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133998478-C-A

126554807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133998616-T-C

126554838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133998651-T-C

126554878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133998694-A-G

126555309-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133999069-A-T

126556376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133999709-G-A

126556376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133999709-G-T

126556749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134000062-C-T

126556865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134000149-G-A

http://identifiers.org/hco/10/GRCh38#126556884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134000173-C-A

http://identifiers.org/hco/10/GRCh38#126557252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134000350-C-A

126557252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134000350-C-T

126557277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134000396-T-C

126557277-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134000396-T-G

126557306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134000425-C-T

126557824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134000888-G-T

126558099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134001515-C-T

126558125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134001539-C-T

126558368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134001782-A-G

126558497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134001893-C-T

126558657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134002224-G-A

126558701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134002345-C-T

126558756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134002423-T-C

126558839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134002516-T-C

http://identifiers.org/hco/10/GRCh38#126559064-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134002741-A-C

126559064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134002741-A-G

126559094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134002764-C-T

126559976-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134005175-T-A

126560058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134005375-G-A

126560112-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134005428-T-G

126560409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134005750-G-A

126560409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134005750-G-T

126560763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134006061-T-C

126561160-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134007050-G-C

126561337-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134007218-C-G

126561563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134007452-A-G

126561603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134007495-C-T

126561874-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134007781-T-A

http://identifiers.org/hco/10/GRCh38#126561927-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134007832-A-C

126561993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134007892-G-A

126561993-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134007892-G-C

126561993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134007892-G-T

126562087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134007987-G-A

126562138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134008038-G-A

126562202-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134008099-A-T

126562207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134008102-A-G

126562268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134008162-A-G

126563590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134010619-C-T

126563672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134010692-C-T

126563725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134010746-G-A

126563779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134010781-G-A

126563790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134010793-G-A

http://identifiers.org/hco/10/GRCh38#126563796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134010799-C-A

126563961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134010890-C-T

126564062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134010988-A-G

126564115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134011061-G-A

126564161-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134011107-T-A

126564200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134011146-A-G

126564216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134011152-T-C

126564320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134011236-G-A

126564642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134011820-C-T

126564645-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134011823-T-A

126569133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134013241-T-C

126569181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134013289-G-T

126569402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134013462-C-T

126569543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134013584-T-C

126569721-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134013756-G-C

126569767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134013797-C-T

126570029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 134014165-C-T

126570112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 134014249-G-A

126570169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134014304-T-C

126570180-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134014313-T-A

126570280-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134014410-T-A

126570320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134014448-C-T

126570765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134014879-G-A

126570775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134014889-A-G

126570799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134014910-C-G

126570799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134014910-C-T

126571059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134015208-G-A

126571059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134015208-G-T

126571133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134015281-A-G

126571190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 134015342-G-A

126571432-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134015544-C-G

126571516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134015622-G-A

126571593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134015702-G-A

126571593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134015702-G-T

http://identifiers.org/hco/10/GRCh38#126571735-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134015825-A-C

http://identifiers.org/hco/10/GRCh38#126571869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134015940-C-A

126571880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134015951-G-T

http://identifiers.org/hco/10/GRCh38#126571906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134015974-C-A

http://identifiers.org/hco/10/GRCh38#126573765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134016282-C-A

126573765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134016282-C-T

126573934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134016428-C-G

http://identifiers.org/hco/10/GRCh38#126574053-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134016552-A-C

126574053-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134016552-A-T

126574054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134016553-C-T

126574125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134016626-G-A

126574191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134016692-A-G

126574191-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134016692-A-T

126574264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134016765-T-C

126578958-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134018511-G-C

126579003-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134018552-T-A

126579003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134018552-T-C

126579003-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134018552-T-G

126579010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134018559-G-A

126579681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134018924-G-A

http://identifiers.org/hco/10/GRCh38#126579705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134018946-C-A

126579705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134018946-C-T

126579706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134018947-A-G

http://identifiers.org/hco/10/GRCh38#126579740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134018981-C-A

126579740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134018981-C-T

126579786-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134019000-T-G

126579918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134019089-T-C

126580082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134019252-C-T

http://identifiers.org/hco/10/GRCh38#126580164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134019318-C-A

126580164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134019318-C-T

http://identifiers.org/hco/10/GRCh38#126580330-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134019485-A-C

126581124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134019988-T-C

126581145-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134020009-C-G

http://identifiers.org/hco/10/GRCh38#126581204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134020059-C-A

126581393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134020254-G-A

126581693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134020776-G-A

126581844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134020917-G-A

http://identifiers.org/hco/10/GRCh38#126582379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134021385-C-A

126582379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134021385-C-T

126582432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134021443-G-A

126582432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134021443-G-T

126582501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134021487-T-C

126582534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134021518-C-T

126582646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134021603-C-T

126582670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134021625-T-C

126582804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134021759-C-T

126582998-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134021942-T-G

126585641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134023575-G-C

http://identifiers.org/hco/10/GRCh38#126585653-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134023584-A-C

126585654-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134023585-T-A

126585654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134023585-T-C

126585884-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134023786-T-G

126585896-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134023799-G-C

126585968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134023889-T-C

126586057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134023968-T-C

http://identifiers.org/hco/10/GRCh38#126586068-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134023979-A-C

126586238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134024492-A-G

126586249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134024504-C-T

126586268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134024523-T-C

126586271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134024526-G-A

126586301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134024556-A-G

126586345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134024598-A-G

126586377-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134024630-C-G

http://identifiers.org/hco/10/GRCh38#126586437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134024676-C-A

126586506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134024753-C-T

126586521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134024765-G-A

126586719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134024957-A-G

126586802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134025017-G-A

126586802-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134025017-G-C

http://identifiers.org/hco/10/GRCh38#126595178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134029526-C-A

http://identifiers.org/hco/10/GRCh38#126595310-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134029657-A-C

126595687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134030031-A-G

126595836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134030181-C-T

http://identifiers.org/hco/10/GRCh38#126598291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#134033624-C-A

126598291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 134033624-C-T

126598396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134033788-A-G

126598517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134033905-C-T

126598590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134033984-G-A

126598711-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134034091-C-G

126598740-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134034120-C-G

126598820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134034207-G-T

126598836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134034224-G-A

126598837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134034225-G-A

126598895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134034306-A-G

126599489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134034955-G-A

126599611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 134035101-T-C

126599636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134035130-G-A

126599756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134035248-C-T

126599773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134035265-A-G

126599809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134035300-T-C

126599966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134035441-A-G

126600011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134035486-T-C

126600111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134035561-G-A

126600353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134035712-T-C

126600449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134035780-C-T

http://identifiers.org/hco/10/GRCh38#126600496-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134035825-A-C

126600638-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134035942-T-A

126600638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134035942-T-C

126600707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134036008-A-G

126600734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134036064-G-A

126601597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134036855-A-G

126601601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134036859-A-G

126601756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134037011-C-T

126601919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134037164-C-T

126601967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134037198-T-C

126601977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134037208-G-A

126602014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134037244-G-A

126602014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134037244-G-T

126602037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134037264-G-T

126602047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134037274-C-T

126602048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134037275-G-A

126602051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134037278-C-T

126602175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134037395-A-G

http://identifiers.org/hco/10/GRCh38#126602216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134037434-C-A

126602216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134037434-C-T

126604116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134037955-A-G

126604136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134037975-G-A

126604136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134037975-G-T

126604236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134038065-C-T

126604238-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134038067-T-A

126604314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134038153-A-G

126604374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134038219-C-T

http://identifiers.org/hco/10/GRCh38#126604751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134038415-C-A

126604822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134038486-T-C

126605075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134038709-T-C

126605103-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134038735-G-C

126606305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134041026-G-C

126606918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134041379-C-T

126606924-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134041385-C-G

126607024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134041416-T-C

126607130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134041496-G-A

126607241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134041616-C-G

126607354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134041728-G-A

126607592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134041967-T-C

126607732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134042098-A-G

126607879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134042235-C-T

126607953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134042291-A-G

126607984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134042315-G-A

126613857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134043276-A-G

http://identifiers.org/hco/10/GRCh38#126614207-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134043534-A-C

126614374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134043693-T-C

126614416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134043734-G-A

126614464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134043774-G-A

126614505-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134043816-T-A

126614703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134043974-G-A

126615014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134044461-A-G

126615101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134044546-G-A

126615112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134044557-G-T

126615123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134044569-G-A

126615243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134044679-T-C

126615317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134044748-A-G

126615562-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134044947-T-A

http://identifiers.org/hco/10/GRCh38#126615745-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134045122-A-C

126615807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134045184-T-C

126616179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134045542-G-T

126616269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134045627-T-C

126616298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134045655-G-A

126616298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134045655-G-C

126616466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134045834-A-G

126616466-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134045834-A-T

126616567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134045909-C-T

126616982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134046312-C-T

126617148-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134046461-G-C

126617158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134046472-G-T

126617304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134046590-T-C

http://identifiers.org/hco/10/GRCh38#126617459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134046729-C-A

126617459-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134046729-C-G

126617497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134046758-C-T

126617527-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134046780-C-G

126617844-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134047166-T-G

126617846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134047168-A-G

126618531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134047891-A-G

126618721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134048073-G-T

126618802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134048155-T-C

126621799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134057949-A-G

126621978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134058493-C-T

126622088-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134058580-T-A

126622210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134058689-G-T

126622412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134058853-C-T

126622714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134059146-T-C

126622888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134059368-T-C

126623177-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134059599-T-G

http://identifiers.org/hco/10/GRCh38#126623248-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134059621-A-C

126623248-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134059621-A-T

126623357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134059719-G-A

126623449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134059797-G-A

126623552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134059908-C-T

126624357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134060087-G-A

126625114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134060794-A-G

126625121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134060801-C-T

126625129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134060809-A-G

126625142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134060812-G-T

http://identifiers.org/hco/10/GRCh38#126625161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134060827-C-A

126625161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134060827-C-T

http://identifiers.org/hco/10/GRCh38#126625200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134060873-C-A

126625345-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134061015-T-G

126625505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134061130-C-T

126625595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134061205-A-G

126626246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134061290-A-G

126626587-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134061611-T-G

126626723-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134061749-C-G

126626873-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134061913-C-G

126627640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134062361-G-A

http://identifiers.org/hco/10/GRCh38#126627648-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134062369-A-C

126628396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134062897-G-T

126628478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134062965-G-A

126628518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134063005-C-T

126628810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134063275-C-T

126628851-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134063313-A-T

126628918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134063523-T-C

126629222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134064014-G-A

126629285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134064075-G-T

126629375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134064165-C-T

126629482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134064272-C-T

126629582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134064371-C-T

126630040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134065213-T-C

126630206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134065367-G-A

http://identifiers.org/hco/10/GRCh38#126630241-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134065401-A-C

126630241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134065401-A-G

126630257-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134065423-T-A

126630338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134065468-T-C

126630366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134065496-G-A

126630477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134065607-G-A

126630479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134065609-G-A

126630561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134065681-G-A

126633736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134065856-C-T

126634983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134066184-C-T

126635008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134066213-T-C

126635028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134066233-C-T

126635419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134066612-G-A

126635790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134067428-A-G

126636170-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134067806-G-C

126636269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134067883-C-T

126636488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134068057-T-C

126639568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134069828-G-A

126639859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134070098-G-A

126640002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134070242-A-G

126640002-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134070242-A-T

126640080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134070317-C-T

126640144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134070378-C-T

126640148-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134070382-C-G

http://identifiers.org/hco/10/GRCh38#126640260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134070476-C-A

126640266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134070480-A-G

126640278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134070492-G-A

http://identifiers.org/hco/10/GRCh38#126640389-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134070617-A-C

http://identifiers.org/hco/10/GRCh38#126640804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134070950-C-A

126641078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134071216-A-G

126641206-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134071328-T-A

126641206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134071328-T-C

126641274-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134071390-A-T

126641905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134072005-C-T

126642084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134072180-C-T

126644698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134073726-G-T

126644742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134073774-G-A

http://identifiers.org/hco/10/GRCh38#126644878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134073908-C-A

126644878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134073908-C-T

126644879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134073909-C-T

126645643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134074054-A-G

http://identifiers.org/hco/10/GRCh38#126645832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134074251-C-A

126646238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134074668-C-T

http://identifiers.org/hco/10/GRCh38#126646330-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134074770-A-C

126646394-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134074918-A-T

126646410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134074946-A-G

http://identifiers.org/hco/10/GRCh38#126646564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134075084-C-A

126646564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 134075084-C-T

126646635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 134075155-G-T

http://identifiers.org/hco/10/GRCh38#126646638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134075158-C-A

http://identifiers.org/hco/10/GRCh38#126646662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134075180-C-A

http://identifiers.org/hco/10/GRCh38#126646734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134075794-C-A

126646734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134075794-C-T

126646736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134075796-G-A

126646736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134075796-G-T

126647123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134076172-T-C

126647161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134076212-G-A

126647162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134076213-T-C

126648520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134077701-T-C

126648539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134077719-T-C

126648559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134077738-C-T

126648568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134077747-G-A

126648568-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134077747-G-C

126648586-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134077765-T-A

126648632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134077803-T-C

126648761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134077913-G-A

126648778-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134077925-A-T

http://identifiers.org/hco/10/GRCh38#126648989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134078133-C-A

http://identifiers.org/hco/10/GRCh38#126649123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134078219-C-A

126649123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134078219-C-T

126649284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134078355-G-A

126649284-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134078355-G-C

126649387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134078457-C-T

126649624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134078668-A-G

126649656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134078698-G-A

126649754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134078786-T-C

126651748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134081456-G-T

126651841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134081550-T-C

126651872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134081572-C-T

126652159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134083690-T-C

126652184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134083716-G-A

126652189-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134083721-A-T

126652568-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134084089-A-T

126652638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134084159-C-T

126652727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134084250-T-C

126652790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134084306-G-A

126652825-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134084340-G-C

126652835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134084350-T-C

126655843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134084682-A-G

126655860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134084695-A-G

126655909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134084744-C-T

126657126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134086564-G-A

126659055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134088063-G-A

126659244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134088242-C-T

126659246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134088244-A-G

126659368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134088364-C-T

126659404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134088396-T-C

126659405-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134088397-G-C

http://identifiers.org/hco/10/GRCh38#126659474-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134088466-A-C

126659539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134088531-C-T

http://identifiers.org/hco/10/GRCh38#126659728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134088700-C-A

126659805-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134088783-T-A

126659874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134088844-T-C

126659989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134088960-G-A

http://identifiers.org/hco/10/GRCh38#126660056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134089013-C-A

126660131-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134089082-T-G

126660153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134089111-C-T

126660154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134089112-G-A

126660196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134089154-G-T

126660240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134089198-G-A

126660292-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134089245-T-A

126660307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134089260-G-A

126660637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134089757-A-G

126660744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134089837-C-T

126660758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134089851-G-T

126660933-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134090043-A-T

126661003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134090080-C-T

126663393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134093083-G-A

126663393-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134093083-G-C

126663592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134093297-G-A

126663592-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134093297-G-C

126665257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134093736-G-A

126665418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134093905-G-A

126665484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134093973-A-G

http://identifiers.org/hco/10/GRCh38#126665517-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134094006-A-C

126666515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134096433-G-A

126666515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134096433-G-T

126667533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134096774-G-A

126667617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134097738-C-T

126667898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134098010-A-G

126667950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134098062-C-T

126667963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134098076-A-G

126668251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134098383-T-C

126668516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134098639-G-A

126668541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134098661-G-A

126668611-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134098992-G-C

126668621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134099002-G-A

126668787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134099170-G-A

126668787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134099170-G-T

126668819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134099202-G-A

http://identifiers.org/hco/10/GRCh38#126668843-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134099223-A-C

126668960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134099341-G-A

126669767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134100142-G-A

126669767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134100142-G-T

http://identifiers.org/hco/10/GRCh38#126669861-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134100220-A-C

126669897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134100256-A-G

126669916-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134100275-A-T

126669927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134100285-C-T

http://identifiers.org/hco/10/GRCh38#126669991-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134100346-A-C

126670197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134100539-T-C

126670209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134100551-G-T

126670212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134100554-C-T

126670349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134100697-C-T

126670412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 134100760-G-A

126670590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134100917-G-T

126670861-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134101183-A-T

126670922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134101244-G-A

126671173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134101481-C-T

126671783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134102060-G-A

126671891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134102164-G-A

126671970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134102236-T-C

http://identifiers.org/hco/10/GRCh38#126671999-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134102261-A-C

126672055-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134102299-A-T

126672080-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134102323-A-T

126672241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134102448-G-A

126672965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134103009-C-T

126673573-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134103541-A-T

126673779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134104628-G-A

126674332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134105537-G-A

126674542-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134105699-G-C

126674563-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134105720-T-A

126674785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134105894-G-A

126674989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134106112-T-C

126675104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134106199-A-G

126675173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134106267-A-G

126675523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134106603-A-G

126675587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134107077-A-G

126675706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134107191-T-C

126675744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134107230-T-C

http://identifiers.org/hco/10/GRCh38#126675779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134107262-C-A

126675891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134107372-C-T

126675998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134107474-T-C

126676220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134107686-G-A

126682696-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134108977-A-T

126682755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134109033-A-G

126682789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134109066-C-T

126683231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134109498-T-C

126683365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134109634-G-A

126683397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134109664-G-A

126683466-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134109732-A-T

126683496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134109754-C-T

126683593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134109854-A-G

126685215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134111260-G-T

126685284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134111317-T-C

126685458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134111441-C-T

126685700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134111624-G-A

126685700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134111624-G-C

126685761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134111679-G-A

126685761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134111679-G-T

126685845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134111779-C-T

126686986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134112240-A-G

126687192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134112390-T-C

http://identifiers.org/hco/10/GRCh38#126687197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134112395-C-A

126687197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134112395-C-T

126687346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134112466-G-A

http://identifiers.org/hco/10/GRCh38#126687364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134112482-C-A

http://identifiers.org/hco/10/GRCh38#126687596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134112706-C-A

126687596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134112706-C-T

126687623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134112733-A-G

126687734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134112859-A-G

126695101-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134114657-G-C

126695356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134115297-T-C

126695716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134115626-C-T

126695917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134115833-C-T

126696507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134116336-T-C

126696590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134116407-C-T

126696699-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134116496-T-A

126698052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134117972-G-A

126698103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134118014-G-A

126698385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134118254-A-G

http://identifiers.org/hco/10/GRCh38#126698530-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134118386-A-C

http://identifiers.org/hco/10/GRCh38#126698655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134118520-C-A

126698811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134118681-G-A

http://identifiers.org/hco/10/GRCh38#126699036-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134119220-A-C

126699150-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134119332-C-G

126701912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134120650-C-T

126702160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134120803-C-T

126702261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134120828-A-G

126702290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134120858-G-A

126702362-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134120921-C-G

126702490-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134121048-C-G

126702583-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134121149-T-G

126702989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134121909-T-C

126703463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134122378-G-A

126703463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134122378-G-T

126703467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134122382-A-G

126703743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134122608-A-G

126704133-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134122901-T-G

126704184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134122966-T-C

http://identifiers.org/hco/10/GRCh38#126704522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134124585-C-A

126704588-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134124649-T-G

126704889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134124947-C-T

126704930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134124988-G-A

126705215-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134125236-C-G

126705215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134125236-C-T

126705620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134125618-C-T

126705689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134125690-C-T

126705843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134125840-G-A

126706055-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134126823-C-G

http://identifiers.org/hco/10/GRCh38#126706194-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134126966-A-C

126706220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134126992-T-C

126706228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134127000-C-T

126706312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134127073-G-A

126706312-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134127073-G-C

126706402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134127150-C-T

126706496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134127237-G-A

126706500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134127241-G-A

126706737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134127464-G-A

126706768-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134127482-T-G

126706804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134127518-G-A

126707187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134128911-A-G

126707219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134128918-C-T

126707523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134129194-G-A

126707597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134129256-T-C

126709618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134134882-A-G

126709739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134135010-C-T

126718288-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134136624-C-G

126718317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134136653-A-G

126718325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134136661-G-A

126718353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134136688-T-C

126718359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134136694-T-C

126718475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134136807-C-T

126718496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134136839-G-A

126718496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134136839-G-T

http://identifiers.org/hco/10/GRCh38#126718997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134137321-C-A

126719222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134138423-G-A

126719250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134138451-T-C

126719291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134138485-A-G

126719291-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134138485-A-T

126719363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134138536-C-T

126719381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134138554-G-T

126719398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134138571-C-T

126719643-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134138803-T-A

http://identifiers.org/hco/10/GRCh38#126719723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134138890-C-A

126719723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134138890-C-T

126719730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134138897-G-A

126719758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134138925-C-T

126719772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134138939-C-T

126719812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134138976-C-T

126719858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134139123-G-A

126719879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134139144-C-T

126720235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134141430-T-C

http://identifiers.org/hco/10/GRCh38#126720323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134141488-C-A

126720444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134141796-T-C

126720465-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134141831-C-G

126720798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134142148-G-A

126720846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134142193-T-C

126720960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134142240-T-C

126721099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134142444-C-T

126721120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134142465-G-A

http://identifiers.org/hco/10/GRCh38#126721469-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134143054-A-C

http://identifiers.org/hco/10/GRCh38#126721658-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134143242-A-C

126721661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134143245-G-A

126722012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134143587-T-C

126722054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134143633-A-G

126722171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134143736-G-A

126722223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134143787-G-A

126722310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134143862-G-A

126722376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134143936-T-C

126722907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134145554-A-G

http://identifiers.org/hco/10/GRCh38#126722957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134145605-C-A

126722957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134145605-C-T

126723296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134145912-C-T

126723316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134145927-G-A

126723345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134145957-G-A

126723365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134145969-T-C

http://identifiers.org/hco/10/GRCh38#126723379-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134145984-A-C

126723526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134146121-A-G

126723580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134146180-G-A

126724962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134146845-C-T

126725010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134146889-G-A

126725066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134146944-G-T

126733827-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134150979-T-G

126733940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134151097-C-T

126734076-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134151218-A-T

126734223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134151362-C-T

126734312-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134151501-G-C

126734459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134151643-C-T

126734661-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134151773-G-C

126734880-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134152000-T-A

126734976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134152096-C-T

126734978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134152098-C-T

126734979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134152099-A-G

126734984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134152104-C-T

126734992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134152112-G-A

126734992-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134152112-G-C

126735181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134152308-G-A

126735251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 134152374-A-G

http://identifiers.org/hco/10/GRCh38#126735357-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134152479-A-C

126735357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134152479-A-G

126735796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134152912-G-A

126735796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134152912-G-T

126735798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134152914-A-G

126735982-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134153755-G-C

126736032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134153807-T-C

126736041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134153816-A-G

126736251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134154001-T-C

126736251-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134154001-T-G

126736362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134154064-C-T

126736688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134154402-G-T

http://identifiers.org/hco/10/GRCh38#126737173-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134154721-A-C

126737182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134154728-C-T

126737313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134154841-C-T

http://identifiers.org/hco/10/GRCh38#126737629-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134155129-A-C

126737938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134155557-C-T

126737940-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134155559-T-A

126738032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134155785-C-T

http://identifiers.org/hco/10/GRCh38#126738293-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134156035-A-C

126738491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134156237-C-T

http://identifiers.org/hco/10/GRCh38#126738838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134156648-C-A

126739294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134158526-G-A

126739311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134158541-T-C

126739558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134158767-G-T

126739590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134161181-G-A

126739590-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134161181-G-C

126739615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134161205-G-T

126739707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134159325-G-A

http://identifiers.org/hco/10/GRCh38#126739947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#134159571-C-A

126739972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134159593-T-C

126740048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134159685-T-C

126740231-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134160178-A-T

126740825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134160762-G-A

126740825-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134160762-G-C

126740878-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134160815-T-A

126741373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134162254-C-T

126741374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134162255-G-A

126741374-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134162255-G-C

126741374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134162255-G-T

126741883-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134163134-G-C

126742474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134163860-A-G

126742527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134163912-G-T

126742951-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134164329-C-G

126743261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134164599-T-C

126743432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26563
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134164784-G-A