139230371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 5 prime UTR variant
orthologous variants: 38410038-G-T

139230474-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38410140-C-G

139230474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38410140-C-T

139230541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38410205-G-C

139230851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38410460-A-G

139230874-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38410485-C-G

139230874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38410485-C-T

139230922-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron_variant, undefined
orthologous variants: 38410532-T-G

139231107-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron_variant, undefined
orthologous variants: 38410730-C-G

139231107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron_variant, undefined
orthologous variants: 38410730-C-T

139231303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 38410926-C-T

139231655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 38411242-T-C

139231675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron_variant, missense_variant
orthologous variants: 38411262-A-G

http://identifiers.org/hco/7/GRCh38#139231680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38411267-C-A

139231680-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron_variant, missense_variant
orthologous variants: 38411267-C-G

139231680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron_variant, missense_variant
orthologous variants: 38411267-C-T

139231862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 38411443-G-A

139231862-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 38411443-G-C

139231862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 38411443-G-T

139232667-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38412196-C-G

139232667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38412196-C-T

139233713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38413484-C-T

139234046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38413805-A-G

139234086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38413845-G-A

139234114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38413870-A-G

139234587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38414617-A-G

139234674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38414691-A-G

139234872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38414878-A-G

139235637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38415555-C-G

139235637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38415555-C-T

139235925-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38415862-C-G

http://identifiers.org/hco/7/GRCh38#139236730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38417120-C-A

139236884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38417281-A-G

139236903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38417301-A-G

139236907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38417305-T-C

139236982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38417367-T-C

139236982-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38417367-T-G

http://identifiers.org/hco/7/GRCh38#139237211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38417593-C-A

139237214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38417596-T-C

139237874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38417947-A-G

139237907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38417969-T-C

139242501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38419785-A-G

139242571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38420509-G-A

139242665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38420591-T-C

139242816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38420732-G-A

http://identifiers.org/hco/7/GRCh38#139243385-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38421448-A-C

139245261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38422153-C-T

http://identifiers.org/hco/7/GRCh38#139245460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38422333-C-A

139245460-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38422333-C-G

139245523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38422391-A-G

139245913-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38422766-T-G

139246054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38422904-T-C

139246065-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38422908-G-C

139246090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38422931-C-T

139246554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38423174-A-G

139246787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38423390-T-C

139247695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38425748-G-T

139251855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38429700-G-A

139251855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38429700-G-C

http://identifiers.org/hco/7/GRCh38#139251881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38429726-C-A

139251881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38429726-C-T

139251939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38429788-G-A

http://identifiers.org/hco/7/GRCh38#139252229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38430030-C-A

139252229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38430030-C-T

139252591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38430367-G-A

139252621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38430395-G-T

139252665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38430440-C-T

139253571-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38432257-C-G

139253809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38432501-A-G

139253995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38432665-G-A

139255989-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38435096-T-A

139255993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38435100-G-A

139256808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38435649-A-G

139258213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38437364-G-A

139258218-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38437369-G-C

139258320-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38437463-T-A

http://identifiers.org/hco/7/GRCh38#139258343-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38437486-A-C

139258343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38437486-A-G

139258361-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38437509-T-A

http://identifiers.org/hco/7/GRCh38#139258363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38437511-C-A

139258363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38437511-C-T

139258367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38437515-T-C

139258415-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38438336-G-C

139258415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38438336-G-T

139258463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38438391-G-A

139258463-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38438391-G-C

139258463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38438391-G-T

http://identifiers.org/hco/7/GRCh38#139258604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38438526-C-A

139258604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: synonymous variant
orthologous variants: 38438526-C-T

139259141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38439777-A-G

139259263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 38439894-G-A

139259263-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 38439894-G-C

http://identifiers.org/hco/7/GRCh38#139259412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38440041-C-A

139259421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38440050-T-C

139259421-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38440050-T-G

http://identifiers.org/hco/7/GRCh38#139259422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38440051-C-A

139259422-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38440051-C-G

139259422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38440051-C-T

139259585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38440173-G-T

139261423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: synonymous variant
orthologous variants: 38440660-A-G

139261468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: synonymous variant
orthologous variants: 38440705-G-T

139261573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: synonymous variant
orthologous variants: 38440810-C-T

139261696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: synonymous variant
orthologous variants: 38440933-G-A

139261696-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: missense variant
orthologous variants: 38440933-G-C

139261705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: synonymous variant
orthologous variants: 38440942-T-C

139263802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38445867-A-G

139264188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38446476-A-G

139264188-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38446476-A-T

139267980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38448112-C-T

139268081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38448215-A-G

139268199-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38448333-T-A

139269381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38455965-C-T

139269384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38455968-T-C

139269663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38456252-A-G

139271675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38457995-A-G

139271832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38458134-G-A

http://identifiers.org/hco/7/GRCh38#139272220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38458638-C-A

139272220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38458638-C-T

139272258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38458674-G-T

139272405-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: missense variant
orthologous variants: 38458822-G-C

139273074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38459237-C-T

139273118-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38459280-T-A

139273122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38459284-T-C

139273213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38459373-G-T

139273274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38459414-T-C

139273491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38459611-A-G

139273817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38459906-A-G

139273817-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38459906-A-T

139274024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: synonymous variant
orthologous variants: 38460147-T-C

139274137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38460260-A-G

http://identifiers.org/hco/7/GRCh38#139276155-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38461068-A-C

139276157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38461070-T-C

139276168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38461081-G-A

139276168-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38461081-G-C

139276168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38461081-G-T

139279132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38463874-A-G

139279270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38463994-G-A

139279270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38463994-G-T

139279286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38464010-T-C

139279295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38464019-C-T

http://identifiers.org/hco/7/GRCh38#139279368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38464093-C-A

139279368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 38464093-C-T

http://identifiers.org/hco/7/GRCh38#139279495-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38464216-A-C

139279527-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38464235-T-A

139279572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38464266-A-G

http://identifiers.org/hco/7/GRCh38#139279627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38464315-C-A

139281764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38465959-G-A

139281764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38465959-G-T

http://identifiers.org/hco/7/GRCh38#139281867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38466057-C-A

139281965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38466148-G-A

139281973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38466156-A-G

139282047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron_variant, missense_variant
orthologous variants: 38466231-A-G

139282111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38466287-G-A

139282111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38466287-G-T

http://identifiers.org/hco/7/GRCh38#139282159-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38466333-A-C

139282264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38466441-C-T

139282547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38466705-G-A

139282958-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38467250-T-G

139283092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: synonymous variant
orthologous variants: 38467387-G-A

139283458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: synonymous variant
orthologous variants: 38467753-C-T

139284037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: synonymous variant
orthologous variants: 38468329-G-A

139284046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: synonymous variant
orthologous variants: 38468338-A-G

139284129-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: missense variant
orthologous variants: 38468421-T-G

139284149-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: missense variant
orthologous variants: 38468441-A-T

139284376-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: synonymous_variant, undefined
orthologous variants: 38468668-T-G

139284639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38468920-G-A

139286439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38470831-C-T

139286639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38471033-A-G

139287053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38471670-G-C

139287115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38471750-G-A

139287629-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38472600-A-T

139287701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38472662-G-T

139287938-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38472879-G-C

139288177-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38473094-A-T

139288211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38473138-G-A

139288345-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38473280-T-A

http://identifiers.org/hco/7/GRCh38#139288520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38473419-C-A

139288520-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38473419-C-G

139288589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38473467-A-G

139288589-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38473467-A-T

http://identifiers.org/hco/7/GRCh38#139289860-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38474050-A-C

139290582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38474356-T-C

139290638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38474401-G-A

139293042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38475373-G-T

139293182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38475569-A-G

139293182-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38475569-A-T

http://identifiers.org/hco/7/GRCh38#139293842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38476081-C-A

139293842-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38476081-C-G

139293972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38476202-G-A

http://identifiers.org/hco/7/GRCh38#139293988-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38476218-A-C

139293989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 38476219-C-T

139294040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38476263-A-G

139294040-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38476263-A-T

http://identifiers.org/hco/7/GRCh38#139294056-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38476278-A-C

139294056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38476278-A-G

139294056-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38476278-A-T

139294076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38476300-G-A

139294076-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38476300-G-C

139294076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38476300-G-T

http://identifiers.org/hco/7/GRCh38#139294115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38476381-C-A

139294115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38476381-C-T

139294135-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38476399-T-A

139294137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38476401-T-C

139295124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38477037-A-G

139295124-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38477037-A-T

139295135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38477048-A-G

139295148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38477061-C-T

139295352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38477200-A-G

139295506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38477289-A-G

139295506-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38477289-A-T

139295610-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38477380-A-T

139296539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38478391-T-C

http://identifiers.org/hco/7/GRCh38#139297364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38478818-C-A

139297895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38479279-G-A

139297895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38479279-G-T

139298090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38479460-G-A

139298090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38479460-G-T

139298425-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38479830-T-G

http://identifiers.org/hco/7/GRCh38#139299075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38480515-C-A

139299144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38480578-G-T

139299513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38480925-T-C

http://identifiers.org/hco/7/GRCh38#139299776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38481888-C-A

139299776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38481888-C-T

139300314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38482305-G-T

139300593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38482535-A-G

139300695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38482634-G-A

http://identifiers.org/hco/7/GRCh38#139300928-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38482873-A-C

139300995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38482937-G-A

http://identifiers.org/hco/7/GRCh38#139301043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38482985-C-A

139301144-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38483088-T-G

http://identifiers.org/hco/7/GRCh38#139301414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38483355-C-A

139301414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38483355-C-T

http://identifiers.org/hco/7/GRCh38#139301760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38483659-C-A

139302273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38484163-A-G

139302805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38484430-A-G

139303082-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38484702-A-T

139303187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38484785-A-G

139303490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38485051-G-A

139303505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38485070-G-A

139303505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38485070-G-T

139304067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38485629-T-C

http://identifiers.org/hco/7/GRCh38#139304101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38485656-C-A

139304104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38485659-G-A

139304166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38485711-G-A

139304166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38485711-G-T

139304181-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38485728-C-G

139304188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38485735-C-T

139304229-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38485767-T-G

139304531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38486039-G-A

139305002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38486446-G-A

139305028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38486471-T-C

http://identifiers.org/hco/7/GRCh38#139305040-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38486482-A-C

139305306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38486735-G-T

139305660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38487066-G-A

139305693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38487099-G-T

http://identifiers.org/hco/7/GRCh38#139305981-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38487565-A-C

http://identifiers.org/hco/7/GRCh38#139306276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38487788-C-A

139306276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38487788-C-T

139306311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38487823-G-A

139306311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38487823-G-T

http://identifiers.org/hco/7/GRCh38#139306366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38487861-C-A

139306366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38487861-C-T

139306368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38487863-T-C

http://identifiers.org/hco/7/GRCh38#139306562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38488055-C-A

139306562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38488055-C-G

139307131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38488587-T-C

139307570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38489047-G-A

139307570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38489047-G-T

139308053-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38489517-A-T

139308118-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38489579-G-C

139308118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38489579-G-T

139308330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38489763-A-G

139308344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38489769-C-T

139315250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38497014-C-T

139315258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21931
most severe consequence: intron variant
orthologous variants: 38497022-A-G