26847767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 5 prime UTR variant
orthologous variants: 30868851-G-A

26847767-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 5 prime UTR variant
orthologous variants: 30868851-G-C

26847767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 5 prime UTR variant
orthologous variants: 30868851-G-T

26847771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 5 prime UTR variant
orthologous variants: 30868855-T-C

26847771-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 5 prime UTR variant
orthologous variants: 30868855-T-G

26847796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 5 prime UTR variant
orthologous variants: 30868886-G-A

26847796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 5 prime UTR variant
orthologous variants: 30868886-G-T

http://identifiers.org/hco/2/GRCh38#26847799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30868889-C-A

26847799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 5 prime UTR variant
orthologous variants: 30868889-C-T

http://identifiers.org/hco/2/GRCh38#26847895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30868995-C-A

26847895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30868995-C-T

http://identifiers.org/hco/2/GRCh38#26847908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30869008-C-A

26847908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30869008-C-T

26848016-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 30869110-T-A

26848016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 30869110-T-C

26848059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 30869155-C-T

26848062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 30869158-A-G

26848087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 30869183-G-A

26848242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 30869334-G-A

26848242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 30869334-G-T

http://identifiers.org/hco/2/GRCh38#26848293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30869387-C-A

26848293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 30869387-C-T

26848296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 30869390-G-A

26848296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 30869390-G-T

26848331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 30869422-G-A

26848371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 30869462-G-A

26848371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 30869462-G-T

26848413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 30869496-G-T

http://identifiers.org/hco/2/GRCh38#26848464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30869540-C-A

26848464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 30869540-C-T

http://identifiers.org/hco/2/GRCh38#26848467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30869543-C-A

http://identifiers.org/hco/2/GRCh38#26848478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30869554-C-A

26848478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 30869554-C-T

http://identifiers.org/hco/2/GRCh38#26848487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30869563-C-A

26848487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 30869563-C-T

26848602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30869680-G-A

26848602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30869680-G-C

26848602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30869680-G-T

26848692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30869780-G-A

26848692-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30869780-G-C

26848773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30869836-C-T

26849235-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30870216-G-C

26849260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, undefined
orthologous variants: 30870242-T-C

26849260-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, undefined
orthologous variants: 30870242-T-G

http://identifiers.org/hco/2/GRCh38#26849338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30870325-C-A

26849850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30870863-C-T

http://identifiers.org/hco/2/GRCh38#26850202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30871178-C-A

26850644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30871613-C-T

26851216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30872078-T-C

26851216-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30872078-T-G

26852163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30873033-G-A

26852475-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30873306-G-C

26852475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30873306-G-T

26852609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30873400-G-A

26852834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30873547-T-C

26852947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30873648-A-G

26853179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30873840-T-C

http://identifiers.org/hco/2/GRCh38#26854621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30875464-C-A

26856008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30876254-C-T

26856852-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30877380-T-G

26859480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30877750-G-A

26859742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30878240-T-C

http://identifiers.org/hco/2/GRCh38#26859902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30878350-C-A

26860215-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30878622-A-T

26862860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30878710-A-G

26862937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30878784-T-C

http://identifiers.org/hco/2/GRCh38#26863109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30878927-C-A

http://identifiers.org/hco/2/GRCh38#26863176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30878999-C-A

26863692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30879555-C-T

26863734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30879593-C-T

http://identifiers.org/hco/2/GRCh38#26863856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30879712-C-A

26863867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30879723-C-G

26863905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30879760-A-G

26863950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30879827-A-G

26864713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30880649-A-G

26864751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30880685-C-T

26864853-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30880784-T-G

26864996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30880922-C-T

26865234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30881147-G-A

26865245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30881158-A-G

26865958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30881552-G-A

26866246-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30881714-T-G

http://identifiers.org/hco/2/GRCh38#26867060-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30882551-A-C

26867224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30882698-G-A

26867233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30882707-G-A

26867269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30882742-A-G

26867387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30882813-T-C

26874857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30885722-A-G

26875246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30886104-G-T

26875521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30886621-A-G

26875530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30886630-G-C

26878285-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30888174-T-A

26878324-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30888211-T-A

26878404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30888293-T-C

26878674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30888542-T-C

26878758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30888624-G-A

26879156-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30889360-G-C

26879475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30889558-A-G

26879681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30889762-G-T

26880319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30890007-C-T

26880385-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30890035-T-A

http://identifiers.org/hco/2/GRCh38#26880571-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30890179-A-C

26880720-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30890286-G-C

26880996-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30890482-T-G

26881031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30890519-G-A

26881190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30890659-C-T

26881193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30890662-C-T

26883393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30891044-G-T

26883974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30891513-G-A

26884050-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30891576-T-G

26884085-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30891610-T-A

26884095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30891620-G-T

26884125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30891652-G-A

26884167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30891684-G-T

26884242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30891757-G-A

26884282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30891800-G-T

26884386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30891862-C-T

26884484-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30891942-G-C

http://identifiers.org/hco/2/GRCh38#26884500-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30891967-A-C

http://identifiers.org/hco/2/GRCh38#26884517-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30891984-A-C

26884517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30891984-A-G

26884925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30892363-A-G

26885170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30892415-G-T

26885501-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30892643-C-G

26885544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30892687-C-T

26886236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30893825-T-C

26886540-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30894059-T-A

26886552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30894071-A-G

http://identifiers.org/hco/2/GRCh38#26886777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30894723-C-A

26887108-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30895165-A-T

26887279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30895440-T-C

http://identifiers.org/hco/2/GRCh38#26887299-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30895460-A-C

http://identifiers.org/hco/2/GRCh38#26887328-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30895478-A-C

26887328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30895478-A-G

26887778-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30895905-G-C

26888000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30896099-C-T

26888645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30896305-A-G

http://identifiers.org/hco/2/GRCh38#26888691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30896351-C-A

26888691-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30896351-C-G

26888749-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30896400-G-C

26888762-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30896413-T-G

26888913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30896559-G-A

26888934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30896585-G-A

26889035-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30896683-C-G

26889190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30896853-A-G

26889196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30896861-G-A

26889870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30897133-C-T

26889921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30897185-T-C

26890000-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30897259-G-C

http://identifiers.org/hco/2/GRCh38#26890020-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30897279-A-C

26890779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30897954-G-A

26891457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30898481-G-A

26892046-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30898919-A-T

26892116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30898987-G-A

http://identifiers.org/hco/2/GRCh38#26892123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30898994-C-A

26892123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30898994-C-G

26892392-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30899220-G-C

26892421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30899252-C-T

26892426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30899257-G-T

26892842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30899533-A-G

26892902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30899600-T-C

26892963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30899648-G-A

26893034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30899709-C-T

http://identifiers.org/hco/2/GRCh38#26893172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30899830-C-A

26893211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30899872-G-A

26898266-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30902338-A-T

26898350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30902408-T-C

26898350-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30902408-T-G

26898351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30902409-G-T

26898354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30902412-A-G

26898424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30902482-T-C

26898451-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30902509-C-G

26898520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: synonymous variant
orthologous variants: 30902590-C-T

26898652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: synonymous variant
orthologous variants: 30902722-T-C

26898679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: synonymous variant
orthologous variants: 30902749-T-C

26898820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30902884-G-T

26898880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30902943-G-C

26898880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30902943-G-T

26898911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30902974-A-G

26898921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30902982-G-A

26898964-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30903018-T-G

26898981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30903035-A-G

26899058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30903106-G-A

26899253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30903578-G-T

http://identifiers.org/hco/2/GRCh38#26899379-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30903710-A-C

http://identifiers.org/hco/2/GRCh38#26899433-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30903740-A-C

26899438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30903745-T-C

26899474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30903784-A-G

http://identifiers.org/hco/2/GRCh38#26899624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30904774-C-A

26899624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30904774-C-T

26899681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30904842-C-T

26900139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30905464-A-G

26900239-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30905552-G-C

26900458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30905933-C-T

26900505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30905983-G-A

26900584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30906057-T-C

26900881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30906366-C-T

26900988-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30906476-C-G

26901139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30906627-G-A

26901383-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30906982-C-G

26901772-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30907351-C-G

26901772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30907351-C-T

26902113-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30907632-T-G

26902158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30907677-C-T

26903462-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30908414-C-G

26903530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30908474-G-A

26904102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30909021-G-A

26904103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30909022-G-A

26904115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30909034-C-T

http://identifiers.org/hco/2/GRCh38#26904489-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30909393-A-C

26904489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30909393-A-G

http://identifiers.org/hco/2/GRCh38#26904567-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30909471-A-C

26904592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30909495-A-G

http://identifiers.org/hco/2/GRCh38#26904628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30909530-C-A

26904628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30909530-C-T

26905106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30910024-A-G

http://identifiers.org/hco/2/GRCh38#26905509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30910608-C-A

http://identifiers.org/hco/2/GRCh38#26905520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30910619-C-A

26905520-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30910619-C-G

26905641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30910751-A-G

26905786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30910838-G-A

26905913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30910956-A-G

26905913-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30910956-A-T

26906017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30911047-G-A

26907428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30912083-T-C

26908444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30913291-A-G

26908575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30913447-G-A

26912086-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30919979-C-G

26912155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30920040-G-A

26912204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30920094-A-G

26912373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30920391-G-A

26912435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30920475-T-C

26912501-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, undefined
orthologous variants: 30920542-T-G

26912537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, undefined
orthologous variants: 30920578-G-A

26912586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, undefined
orthologous variants: 30920635-C-T

26912614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, undefined
orthologous variants: 30920663-C-T

26912662-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, undefined
orthologous variants: 30920712-T-A

26912686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, undefined
orthologous variants: 30920729-G-A

26912727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, undefined
orthologous variants: 30920770-G-A

26912727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, undefined
orthologous variants: 30920770-G-T

26912817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30920860-C-T

26912926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30920964-C-T

26913039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30921093-G-T

http://identifiers.org/hco/2/GRCh38#26913242-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30921256-A-C

26913407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30921407-C-T

26913592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30921576-T-C

26913649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30922755-A-G

26913913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30922999-C-T

26914428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30923423-T-C

26914663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30923678-C-T

26914688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30923703-C-T

26915764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30925608-T-C

26915775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30925619-G-A

26915850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30925686-T-C

26916466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30926260-C-T

26916791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30926529-A-G

26917031-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30926749-G-C

26917041-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30926759-T-G

26918425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30927759-G-A

26918582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30927908-T-C

26918616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30927942-G-A

26918616-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30927942-G-C

26919019-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30928679-C-G

http://identifiers.org/hco/2/GRCh38#26919150-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30928777-A-C

http://identifiers.org/hco/2/GRCh38#26919161-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30928787-A-C

26919186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30928803-G-A

26919236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30928861-A-G

http://identifiers.org/hco/2/GRCh38#26919761-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30929642-A-C

http://identifiers.org/hco/2/GRCh38#26919836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30929715-C-A

26919836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30929715-C-T

26921450-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30931468-T-G

http://identifiers.org/hco/2/GRCh38#26921768-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30931663-A-C

26922031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30931868-G-A

26922044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30931881-T-C

26922060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30931898-T-C

26922293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30932127-G-A

26922659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30932403-A-G

26922763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30932495-A-G

26922770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30932502-T-C

26922789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, undefined
orthologous variants: 30932521-C-T

26924706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30934469-G-A

26924777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30934531-T-C

26924782-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30934536-A-T

26924788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30934550-G-A

26924788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30934550-G-T

http://identifiers.org/hco/2/GRCh38#26924816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30934590-C-A

26924835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30934609-G-T

26925068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30934856-A-G

26925135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30934934-G-A

26925135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30934934-G-T

26925155-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30934954-T-A

26925185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, undefined
orthologous variants: 30934981-A-G

http://identifiers.org/hco/2/GRCh38#26925197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#30934993-C-A

26925208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, undefined
orthologous variants: 30935004-G-A

26925226-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30935022-C-G

http://identifiers.org/hco/2/GRCh38#26925310-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#30935109-A-C

26927405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: synonymous variant
orthologous variants: 30935471-T-C

http://identifiers.org/hco/2/GRCh38#26927523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30935564-C-A

26927523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30935564-C-T

26927554-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30935602-T-A

26927563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30935611-G-A

26927563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30935611-G-T

26927630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30935666-C-T

26927716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30935734-G-A

26927780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30935799-G-A

26927807-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30935822-C-G

26927885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30935887-G-T

26928918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30937020-G-A

26929859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30937265-C-T

26930094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30937595-C-T

26930141-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30937633-T-G

26930168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30937661-G-A

http://identifiers.org/hco/2/GRCh38#26930246-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30937930-A-C

26930265-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30937953-T-A

26930352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30938037-G-A

26930456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30938140-T-C

26930507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30938196-G-A

26930515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30938205-A-G

26931173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30938405-G-A

26931199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30938431-G-A

26931199-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30938431-G-C

26931416-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30938599-A-T

http://identifiers.org/hco/2/GRCh38#26931489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30938672-C-A

26931489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30938672-C-T

26931500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30938683-G-A

26931500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30938683-G-T

http://identifiers.org/hco/2/GRCh38#26931511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30938687-C-A

26931511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30938687-C-G

26931511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30938687-C-T

26931520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30938696-G-A

26931520-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30938696-G-C

http://identifiers.org/hco/2/GRCh38#26931541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30938723-C-A

http://identifiers.org/hco/2/GRCh38#26931552-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30938736-A-C

26931552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30938736-A-G

26932767-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30940068-C-G

26933064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30940348-G-A

26933074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30940358-G-A

26933170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30940458-T-C

26933176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30940463-G-A

26933190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30940473-G-T

26933210-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30940493-A-T

26933243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30940524-G-A

26933358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30940642-A-G

26933444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30940696-A-G

26933445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30940697-G-A

26933445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30940697-G-T

http://identifiers.org/hco/2/GRCh38#26933451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30940703-C-A

26933451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30940703-C-T

26933453-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30940705-T-A

26933453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30940705-T-C

26933548-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30940784-T-G

26933574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30940810-G-A

26933798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30941029-G-A

26933884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30941084-G-A

26933900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30941100-C-T

26933908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30941108-G-A

26933956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30941155-G-A

26933963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30941162-A-G

26934096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30941258-G-A

26934235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30941379-C-T

26934335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30941455-A-G

http://identifiers.org/hco/2/GRCh38#26934456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30941550-C-A

26934456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30941550-C-T

26934474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30941568-T-C

26934511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30941592-G-T

26934606-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: synonymous variant
orthologous variants: 30941683-T-G

26934618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: synonymous variant
orthologous variants: 30941695-G-A

http://identifiers.org/hco/2/GRCh38#26934648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30941725-C-A

26934954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30942010-G-A

26934954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30942010-G-T

26934996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30942030-G-A

26937213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30943629-T-C

26937368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30943953-T-C

26937522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30944093-T-C

26938195-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30944622-T-G

26938226-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron variant
orthologous variants: 30944641-T-A

http://identifiers.org/hco/2/GRCh38#26938498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30944878-C-A

26938498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30944878-C-T

http://identifiers.org/hco/2/GRCh38#26938506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30944886-C-A

26938614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 30944990-T-C

26938614-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 30944990-T-G

26938677-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30945086-T-G

26938682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30945091-A-G

26938685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30945094-A-G

26938724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 30945186-T-C

http://identifiers.org/hco/2/GRCh38#26938844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30945273-C-A

26938844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30945273-C-T

26938872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30945301-G-A

26938872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30945301-G-T

26938882-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30945311-G-C

26938882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30945311-G-T

26938926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30945332-G-A

26938926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30945332-G-T

http://identifiers.org/hco/2/GRCh38#26939032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30945418-C-A

26939032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30945418-C-T

26939037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30945423-A-G

26939053-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30945438-T-A

26939053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30945438-T-C

http://identifiers.org/hco/2/GRCh38#26939057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30945442-C-A

26939057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30945442-C-T

http://identifiers.org/hco/2/GRCh38#26939061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30945446-C-A

26939105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30945479-G-T

26939663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30945694-G-A

26939686-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30945717-T-A

26939686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30945717-T-C

26939686-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30945717-T-G

26939728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30945759-T-C

26939728-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30945759-T-G

http://identifiers.org/hco/2/GRCh38#26939737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30945768-C-A

26939737-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30945768-C-G

26939751-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30945785-T-A

26939760-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30945794-T-G

http://identifiers.org/hco/2/GRCh38#26939767-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30945801-A-C

26939767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30945801-A-G

http://identifiers.org/hco/2/GRCh38#26939770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30945803-C-A

26939771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30945804-T-C

http://identifiers.org/hco/2/GRCh38#26939814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30945846-C-A

26939814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30945846-C-T

26939817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30945849-A-G

26939828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30945863-G-A

26939828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30945863-G-T

26939943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30945973-A-G

26939950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30945980-G-A

26940121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30946133-T-C

26940125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30946137-G-A

26941408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30947860-G-T

26941444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30947909-G-C

26941810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30948700-G-T

26941817-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30948707-A-T

26941820-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30948710-G-C

http://identifiers.org/hco/2/GRCh38#26941821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30948711-C-A

26941821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30948711-C-T

26941824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30948714-T-C

26941843-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30948734-T-A

26941843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30948734-T-C

http://identifiers.org/hco/2/GRCh38#26941910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30948797-C-A

26941910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30948797-C-T

26941923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30948810-G-A

http://identifiers.org/hco/2/GRCh38#26942030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30948916-C-A

26942066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30948952-G-A

26942239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30949128-T-C

26942306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30949194-C-T

26942431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30949330-G-T

26942489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30949400-T-C

26942493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30949404-A-G

26942618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 30949539-A-G

26942657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30949578-C-T

26942660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30949581-C-T

26942813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30949738-A-G

26942813-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30949738-A-T

26944431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30951079-C-T

26944503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30951157-A-G

26944581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30951218-A-G

26944716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30951338-C-T

http://identifiers.org/hco/2/GRCh38#26944879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30951491-C-A

26944879-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30951491-C-G

26944880-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30951492-T-A

26944880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30951492-T-C

26945036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30951591-G-A

26945036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30951591-G-T

26945076-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30951616-C-G

http://identifiers.org/hco/2/GRCh38#26945203-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30951717-A-C

26945206-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30951720-C-G

26945246-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30951756-C-G

26945246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30951756-C-T

26945248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30951758-C-T

http://identifiers.org/hco/2/GRCh38#26945262-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30951772-A-C

http://identifiers.org/hco/2/GRCh38#26945293-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30951791-A-C

26945293-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30951791-A-T

26945429-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30951912-G-C

26945470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30951955-C-T

http://identifiers.org/hco/2/GRCh38#26945509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30952002-C-A

26945509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30952002-C-T

http://identifiers.org/hco/2/GRCh38#26945526-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30952022-A-C

26945577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30952110-G-A

26945597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30952130-C-T

26945620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30952153-G-A

26945621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30952154-G-A

26945688-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30952202-A-T

26945789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30952277-G-A

26945831-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30952322-C-G

26946114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30952537-C-T

http://identifiers.org/hco/2/GRCh38#26946377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30952808-C-A

26946377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30952808-C-T

26946525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30952875-G-A

26946602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30952954-G-A

26946680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30953023-C-T

http://identifiers.org/hco/2/GRCh38#26946814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30953167-C-A

26946814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30953167-C-T

http://identifiers.org/hco/2/GRCh38#26946886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30953558-C-A

26946886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30953558-C-T

26947039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30953717-A-G

26947040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30953718-G-A

26947040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30953718-G-T

http://identifiers.org/hco/2/GRCh38#26947080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30953760-C-A

26947080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30953760-C-T

26947103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30953782-G-A

26947103-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30953782-G-C

26947103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30953782-G-T

http://identifiers.org/hco/2/GRCh38#26947111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30953790-C-A

26947111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30953790-C-T

26947155-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30953833-C-G

http://identifiers.org/hco/2/GRCh38#26947311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30953986-C-A

26947311-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30953986-C-G

http://identifiers.org/hco/2/GRCh38#26947511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30954192-C-A

26947511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30954192-C-T

26947631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30954330-G-A

26947631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30954330-G-T

http://identifiers.org/hco/2/GRCh38#26947738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30954436-C-A

26947738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30954436-C-T

26947751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30954450-A-G

26947999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30954685-G-A

26947999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30954685-G-T

26948026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30954698-T-C

http://identifiers.org/hco/2/GRCh38#26948040-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30954711-A-C

26948040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30954711-A-G

26948040-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30954711-A-T

26948131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30954762-T-C

26948213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30954844-G-T

26948235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30954874-G-T

26948236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30954875-G-A

26948236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30954875-G-T

26948362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30954969-G-T

http://identifiers.org/hco/2/GRCh38#26948399-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30955006-A-C

26948448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30955028-A-G

http://identifiers.org/hco/2/GRCh38#26949059-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30955327-A-C

26949059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3 prime UTR variant
orthologous variants: 30955327-A-G

26949172-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3 prime UTR variant
orthologous variants: 30955432-T-G

26949242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3 prime UTR variant
orthologous variants: 30955480-T-C

26949242-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3 prime UTR variant
orthologous variants: 30955480-T-G

26949372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3 prime UTR variant
orthologous variants: 30955578-G-T

26949517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3 prime UTR variant
orthologous variants: 30955879-G-T

http://identifiers.org/hco/2/GRCh38#26949590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30955947-C-A

26949622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3 prime UTR variant
orthologous variants: 30955979-G-A

26949622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3 prime UTR variant
orthologous variants: 30955979-G-T

http://identifiers.org/hco/2/GRCh38#26949665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30956022-C-A

26949665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3 prime UTR variant
orthologous variants: 30956022-C-T

http://identifiers.org/hco/2/GRCh38#26949668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30956024-C-A

26949806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3 prime UTR variant
orthologous variants: 30956171-C-T

26949812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3 prime UTR variant
orthologous variants: 30956177-G-A

26949812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3 prime UTR variant
orthologous variants: 30956177-G-T

26949956-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3 prime UTR variant
orthologous variants: 30956320-C-G

26949956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3 prime UTR variant
orthologous variants: 30956320-C-T

26950015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3 prime UTR variant
orthologous variants: 30956379-C-T

26950065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3 prime UTR variant
orthologous variants: 30956430-G-A

26950065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3 prime UTR variant
orthologous variants: 30956430-G-T

26950155-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3 prime UTR variant
orthologous variants: 30956520-T-A

26950155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3 prime UTR variant
orthologous variants: 30956520-T-C

26950250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3 prime UTR variant
orthologous variants: 30956613-G-A

26950250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20637
most severe consequence: 3 prime UTR variant
orthologous variants: 30956613-G-T