http://identifiers.org/hco/1/GRCh38#1335400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155943625-C-A

1335400-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 3 prime UTR variant
orthologous variants: 155943625-C-G

1335400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 3 prime UTR variant
orthologous variants: 155943625-C-T

1335408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 3 prime UTR variant
orthologous variants: 155943617-G-A

1335408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 3 prime UTR variant
orthologous variants: 155943617-G-T

1335412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 3 prime UTR variant
orthologous variants: 155943613-G-A

1335412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 3 prime UTR variant
orthologous variants: 155943613-G-T

1335431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 3 prime UTR variant
orthologous variants: 155943600-G-A

1335431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 3 prime UTR variant
orthologous variants: 155943600-G-T

http://identifiers.org/hco/1/GRCh38#1335449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155943581-C-A

http://identifiers.org/hco/1/GRCh38#1335456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155943574-C-A

1335456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 3 prime UTR variant
orthologous variants: 155943574-C-T

http://identifiers.org/hco/1/GRCh38#1335473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155943557-C-A

1335473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 3 prime UTR variant
orthologous variants: 155943557-C-T

1335539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 3 prime UTR variant
orthologous variants: 155943534-T-C

1335580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 3 prime UTR variant
orthologous variants: 155943496-T-C

1335674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 3 prime UTR variant
orthologous variants: 155943378-G-A

1335674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 3 prime UTR variant
orthologous variants: 155943378-G-T

http://identifiers.org/hco/1/GRCh38#1335711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155943363-C-A

1335711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 3 prime UTR variant
orthologous variants: 155943363-C-T

1335722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 3 prime UTR variant
orthologous variants: 155943352-G-A

http://identifiers.org/hco/1/GRCh38#1335724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155943350-C-A

1335724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 3 prime UTR variant
orthologous variants: 155943350-C-T

http://identifiers.org/hco/1/GRCh38#1335737-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155943337-A-C

1335765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 3 prime UTR variant
orthologous variants: 155943297-G-A

1335765-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 3 prime UTR variant
orthologous variants: 155943297-G-C

1335765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 3 prime UTR variant
orthologous variants: 155943297-G-T

1335782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 3 prime UTR variant
orthologous variants: 155943277-G-A

1335782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 3 prime UTR variant
orthologous variants: 155943277-G-T

1335825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 3 prime UTR variant
orthologous variants: 155943205-G-A

1335825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 3 prime UTR variant
orthologous variants: 155943205-G-T

1336017-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 3 prime UTR variant
orthologous variants: 155942972-T-A

1336017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 3 prime UTR variant
orthologous variants: 155942972-T-C

1336065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 3 prime UTR variant
orthologous variants: 155942894-G-A

1336065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 3 prime UTR variant
orthologous variants: 155942894-G-T

1336069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 3 prime UTR variant
orthologous variants: 155942890-G-A

1336069-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 3 prime UTR variant
orthologous variants: 155942890-G-C

1336069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 3 prime UTR variant
orthologous variants: 155942890-G-T

http://identifiers.org/hco/1/GRCh38#1336097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155942865-C-A

1336097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 3 prime UTR variant
orthologous variants: 155942865-C-T

1336119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 3 prime UTR variant
orthologous variants: 155942845-A-G

1336120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 3 prime UTR variant
orthologous variants: 155942844-G-A

1336120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 3 prime UTR variant
orthologous variants: 155942844-G-T

1336194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 155942769-G-A

1336194-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 155942769-G-C

1336194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 155942769-G-T

1336221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 155942742-G-T

1336242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 155942721-A-G

1336242-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 155942721-A-T

1336379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 155942584-T-C

http://identifiers.org/hco/1/GRCh38#1336490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155942473-C-A

1336518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 155942444-G-A

1336518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 155942444-G-T

1336520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 155942442-G-A

1336520-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 155942442-G-C

1336520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 155942442-G-T

1336595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: 155942373-G-A

1336595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: 155942373-G-T

1336627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: 155942340-G-A

1336627-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: 155942340-G-C

1336627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: 155942340-G-T

1336907-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: 155942088-C-G

1336907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: 155942088-C-T

http://identifiers.org/hco/1/GRCh38#1336950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155942057-C-A

1337194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: 155941829-A-G

1337196-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: 155941827-T-A

1337196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: 155941827-T-C

http://identifiers.org/hco/1/GRCh38#1337202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155941821-C-A

1337228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: 155941795-C-T

1337310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: 155941721-G-A

1337511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: 155941530-G-A

http://identifiers.org/hco/1/GRCh38#1337638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155941454-C-A

http://identifiers.org/hco/1/GRCh38#1337659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155941441-C-A

1337659-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: 155941441-C-G

1337659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: 155941441-C-T

1337745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: 155941389-T-C

1337745-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: 155941389-T-G

1337777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: 155941382-G-A

http://identifiers.org/hco/1/GRCh38#1337785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155941375-C-A

1337797-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: 155941363-T-A

1337847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: 155941339-G-A

1337847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: 155941339-G-T

1337849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: 155941337-A-G

1337850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: 155941336-G-A

1337850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: 155941336-G-T

1337865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: 155941321-G-A

1337865-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: 155941321-G-C

1337865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: 155941321-G-T

1337871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: 155941320-G-A

1337871-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: 155941320-G-C

1337871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: 155941320-G-T

1337872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: 155941319-G-A

1337872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: 155941319-G-T

http://identifiers.org/hco/1/GRCh38#1337930-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155941304-A-C

1337930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: 155941304-A-G

1337968-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: 155941287-C-G

1337968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: 155941287-C-T

1338003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: missense variant
orthologous variants: 155941249-C-T

http://identifiers.org/hco/1/GRCh38#1338009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155941243-C-A

1338009-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: missense variant
orthologous variants: 155941243-C-G

1338010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: missense variant
orthologous variants: 155941242-C-T

1338039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: missense variant
orthologous variants: 155941213-G-A

1338105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: missense variant
orthologous variants: 155941147-G-A

1338129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: missense variant
orthologous variants: 155941123-G-A

1338129-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: missense variant
orthologous variants: 155941123-G-C

1338217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: 155941022-G-T

1338223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: 155941016-C-T

http://identifiers.org/hco/1/GRCh38#1338240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155941000-C-A

1338240-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: 155941000-C-G

1338240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: 155941000-C-T

http://identifiers.org/hco/1/GRCh38#1338241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155940999-C-A

1338241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: 155940999-C-G

1338241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: 155940999-C-T

1338242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: 155940998-G-A

1338242-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: 155940998-G-C

1338242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: 155940998-G-T

http://identifiers.org/hco/1/GRCh38#1338256-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155940997-A-C

1338256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron variant
orthologous variants: 155940997-A-G

1338280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: missense variant
orthologous variants: 155940973-T-C

1338521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 155940719-C-T

1338530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155940710-G-A

1338530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155940710-G-T

1338638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155940602-G-A

1338638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155940602-G-T

1338836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155940517-G-A

1338918-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155940433-G-C

1338958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155940395-C-T

1339183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155940191-G-A

1339183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155940191-G-T

1339212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155940157-G-A

1339330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 155940031-G-A

1339330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 155940031-G-T

1339458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155939902-G-T

http://identifiers.org/hco/1/GRCh38#1339469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155939890-C-A

1339469-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155939890-C-G

1339469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155939890-C-T

1339491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155939878-G-A

1339491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155939878-G-C

1339491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155939878-G-T

1339534-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155939838-T-A

1339534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155939838-T-C

1339536-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155939835-G-C

http://identifiers.org/hco/1/GRCh38#1339577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155939799-C-A

http://identifiers.org/hco/1/GRCh38#1339678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155939692-C-A

1339678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155939692-C-G

1339678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155939692-C-T

http://identifiers.org/hco/1/GRCh38#1339766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155939605-C-A

1339766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155939605-C-T

1339772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155939599-G-A

1339814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 155939557-T-C

1339842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155939528-G-A

1339842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155939528-G-T

1339987-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155939495-C-G

1340190-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155939328-C-G

1340190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155939328-C-T

1340199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155939317-G-A

1340199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155939317-G-T

1340211-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155939305-C-G

1340219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155939297-G-A

1340235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155939267-C-T

1340309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155939193-G-A

1340309-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155939193-G-C

1340309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155939193-G-T

1340311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 155939191-G-A

1340311-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 155939191-G-C

1340312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155939190-G-A

1340312-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155939190-G-C

1340330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155939165-G-A

1340331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155939164-G-A

1340331-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155939164-G-C

http://identifiers.org/hco/1/GRCh38#1340444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155939080-C-A

1340444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: missense variant
orthologous variants: 155939080-C-T

1340461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: synonymous variant
orthologous variants: 155939063-G-A

1341733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: missense variant
orthologous variants: 155938857-G-A

1341733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: missense variant
orthologous variants: 155938857-G-T

1341739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: missense variant
orthologous variants: 155938851-G-A

http://identifiers.org/hco/1/GRCh38#1341849-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155938744-A-C

1341855-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155938738-T-A

1341855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155938738-T-C

1341861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155938732-T-C

1341873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155938720-G-T

1341905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155938677-G-A

1341905-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155938677-G-C

1341905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155938677-G-T

1341909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155938673-G-A

1341909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155938673-G-T

1341929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155938667-G-T

http://identifiers.org/hco/1/GRCh38#1341932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155938664-C-A

1341959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155938637-G-A

1341959-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155938637-G-C

1341959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155938637-G-T

1341986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155938607-G-A

1341986-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155938607-G-C

1341986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155938607-G-T

1342002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155938592-G-A

1342002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155938592-G-T

1342004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155938590-G-A

1342004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155938590-G-T

1342020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155938574-G-T

1342021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155938573-G-A

1342021-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155938573-G-C

http://identifiers.org/hco/1/GRCh38#1342045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155938549-C-A

1342193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155938396-G-A

1342193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155938396-G-T

1342307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155938291-A-G

http://identifiers.org/hco/1/GRCh38#1342517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155938061-C-A

1342616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155937999-G-A

1342616-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155937999-G-C

1342616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155937999-G-T

1342774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155937857-G-A

http://identifiers.org/hco/1/GRCh38#1342776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155937855-C-A

1342776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155937855-C-T

1342791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155937838-G-A

1342791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155937838-G-T

1342803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155937833-C-T

http://identifiers.org/hco/1/GRCh38#1342891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155937806-C-A

1342891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155937806-C-T

http://identifiers.org/hco/1/GRCh38#1342915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155937798-C-A

1343061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155937663-G-T

1343101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155937624-C-T

1343116-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155937609-C-G

1343146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155937582-G-A

1343176-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155937552-C-G

1343277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155937461-C-T

1343599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155937157-C-T

1343655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155937115-A-G

http://identifiers.org/hco/1/GRCh38#1343723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155937050-C-A

1343723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155937050-C-T

1343740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155937036-G-A

1343750-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155937026-T-A

1343921-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155936823-A-T

1343945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155936801-G-A

1344010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155936738-C-T

http://identifiers.org/hco/1/GRCh38#1344631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155936273-C-A

1345109-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 155935946-T-A

1345471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155935585-T-C

1345635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155935363-A-G

1345850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155935152-C-T

1346238-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155934839-C-G

http://identifiers.org/hco/1/GRCh38#1346242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155934835-C-A

1346242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155934835-C-T

1346286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155934791-C-T

1346333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155934753-T-C

1346393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155934695-A-G

1346398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155934690-C-T

1346406-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155934682-T-G

1346482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155934625-C-T

1346526-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155934568-G-C

1346641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155934459-G-A

1346798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155934379-G-A

1346856-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155934315-C-G

1347001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155934265-C-T

1347005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155934261-G-T

1347278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155934060-C-T

1347303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155934027-C-T

1347316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155934006-C-T

1347323-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155933999-C-G

http://identifiers.org/hco/1/GRCh38#1347382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155933942-C-A

1347427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155933904-G-A

1347469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155933874-G-A

1347666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155933722-C-T

1347727-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155933675-G-C

1347848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155933584-C-T

http://identifiers.org/hco/1/GRCh38#1348129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155933280-C-A

1348335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 155933071-A-G

1348504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155932890-G-A

1348518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155932876-G-A

http://identifiers.org/hco/1/GRCh38#1348563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155932810-C-A

1348587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155932789-G-A

http://identifiers.org/hco/1/GRCh38#1348639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155932670-C-A

http://identifiers.org/hco/1/GRCh38#1348658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155932650-C-A

http://identifiers.org/hco/1/GRCh38#1348663-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155932645-A-C

http://identifiers.org/hco/1/GRCh38#1348769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155932507-C-A

1348769-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155932507-C-G

1348769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155932507-C-T

http://identifiers.org/hco/1/GRCh38#1348825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155932446-C-A

http://identifiers.org/hco/1/GRCh38#1348833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155932438-C-A

1348833-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155932438-C-G

1348833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155932438-C-T

1348861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155932391-G-A

1348861-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155932391-G-C

1348861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155932391-G-T

1348911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155932344-A-G

1349260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 5 prime UTR variant
orthologous variants: 155932026-G-A

1349260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 5 prime UTR variant
orthologous variants: 155932026-G-T

1349393-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 155931912-C-G

1349393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 155931912-C-T

1349402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 155931905-G-A

1349402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 155931905-G-T

1349409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 155931898-G-A

1349409-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 155931898-G-C

1349409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3084
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 155931898-G-T