http://identifiers.org/hco/7/GRCh38#2354122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#140404337-C-A

2354122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 140404337-C-T

2354131-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 140404346-T-A

2354131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 140404346-T-C

http://identifiers.org/hco/7/GRCh38#2354173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#140404388-C-A

2354173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 140404388-C-T

2354223-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 140404439-T-A

2354223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 140404439-T-C

2354239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 140404454-G-A

2354239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 140404454-G-T

2354270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 140404483-T-C

2354270-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 140404483-T-G

2354292-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 140404505-T-G

2354334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 140404548-G-A

2354334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 140404548-G-T

2354387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 140404603-G-T

2354489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 140404703-C-T

2354507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: 140404718-C-T

2354526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 140404737-C-T

http://identifiers.org/hco/7/GRCh38#2354561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#140404772-C-A

2354561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 140404772-C-T

2354699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 140404910-A-G

2354701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 140404912-A-G

http://identifiers.org/hco/7/GRCh38#2354783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#140404991-C-A

2354783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 140404991-C-T

http://identifiers.org/hco/7/GRCh38#2354809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#140405016-C-A

2354809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 140405016-C-T

2354838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 140405045-G-A

2354838-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 140405045-G-C

2354838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 140405045-G-T

2355017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 140405211-G-A

2355017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, missense_variant
orthologous variants: 140405211-G-T

http://identifiers.org/hco/7/GRCh38#2355024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140405218-C-A

2355024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 140405218-C-T

2355035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 140405229-G-A

2355035-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 140405229-G-C

2355102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, missense_variant
orthologous variants: 140405278-G-A

2355102-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, missense_variant
orthologous variants: 140405278-G-C

2355102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, missense_variant
orthologous variants: 140405278-G-T

2355116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, splice_region_variant, synonymous_variant
orthologous variants: 140405292-G-A

2355116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 140405292-G-T

http://identifiers.org/hco/7/GRCh38#2355159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140405341-C-A

2355159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, missense_variant
orthologous variants: 140405341-C-T

2355165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, missense_variant
orthologous variants: 140405347-G-A

2355165-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, missense_variant
orthologous variants: 140405347-G-C

2355165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, undefined
orthologous variants: 140405347-G-T

2355167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 140405349-G-A

2355167-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, missense_variant
orthologous variants: 140405349-G-C

2355167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, missense_variant
orthologous variants: 140405349-G-T

http://identifiers.org/hco/7/GRCh38#2355184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140405366-C-A

2355184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, missense_variant
orthologous variants: 140405366-C-T

http://identifiers.org/hco/7/GRCh38#2355314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140405475-C-A

2355314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 140405475-C-T

http://identifiers.org/hco/7/GRCh38#2355398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140405559-C-A

2355398-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 140405559-C-G

2355398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 140405559-C-T

2355433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: 140405601-G-A

2355433-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: 140405601-G-C

2355433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: 140405601-G-T

http://identifiers.org/hco/7/GRCh38#2355437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140405605-C-A

2355437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: 140405605-C-T

2357156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: 140407149-C-T

2357202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: 140407200-G-A

2357249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: 140407251-T-C

2357285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: 140407284-T-C

2357286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: 140407285-G-A

2357320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: 140407314-C-T

2357328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: 140407322-C-T

2357824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: 140407877-C-T

2357825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: 140407878-G-A

2357844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: 140407897-G-T

2357880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: 140407934-G-A

http://identifiers.org/hco/7/GRCh38#2357882-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140407936-A-C

2357884-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: 140407938-C-G

2357895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: 140407949-C-T

2357988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: 140408035-T-C

2360618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: 140410928-G-A

2360618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: 140410928-G-T

2360702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 140411009-T-C

2360702-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 140411009-T-G

2360759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 140411066-C-T

2362500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: 140412064-T-C

2362518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: 140412082-G-A

2362518-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: 140412082-G-C

2362518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: 140412082-G-T

2362561-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: 140412109-G-C

2362561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: 140412109-G-T

2362580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: 140412128-G-A

2362622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: 140412167-G-A

2362699-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 140412246-C-G

2362699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 140412246-C-T

2362792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: 140412318-T-C

2362797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: 140412323-G-A

2362838-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: 140412361-C-G

2362838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: 140412361-C-T

2362884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: 140412410-A-G

2362884-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: 140412410-A-T

http://identifiers.org/hco/7/GRCh38#2362909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140412433-C-A

2362996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: 140412463-C-T

2363028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 140412494-G-A

2363028-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 140412494-G-C

2363028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 140412494-G-T

2363554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140412686-A-G

http://identifiers.org/hco/7/GRCh38#2363601-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140412736-A-C

2363616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140412753-T-C

2363697-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 140412837-T-A

2363724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 140412864-T-C

http://identifiers.org/hco/7/GRCh38#2363775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140412915-C-A

http://identifiers.org/hco/7/GRCh38#2363899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140413047-C-A

2363953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140413100-G-A

2364312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140413106-G-A

http://identifiers.org/hco/7/GRCh38#2366237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140415709-C-A

2366237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140415709-C-T

2366241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140415713-G-A

2366241-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140415713-G-C

2366241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140415713-G-T

2366252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140415724-G-A

2366252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140415724-G-T

2366306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140415796-T-C

2366377-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 140415867-C-G

2366474-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140415966-T-G

2366475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140415967-G-A

2366475-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140415967-G-C

2366512-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140416004-T-A

2366512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140416004-T-C

2367056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140416787-T-C

2367066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140416797-G-C

2367075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140416804-G-A

2367075-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140416804-G-C

2367075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140416804-G-T

2367141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140416840-G-A

2367141-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140416840-G-C

2367141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140416840-G-T

2367148-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140416847-A-T

2367181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140416879-T-C

2367194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140416892-G-A

2367194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140416892-G-T

http://identifiers.org/hco/7/GRCh38#2367211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140416911-C-A

2367211-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140416911-C-G

2367211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140416911-C-T

2369208-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140418429-G-C

http://identifiers.org/hco/7/GRCh38#2369338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140418557-C-A

2369338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140418557-C-T

2369348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140418570-G-A

2369348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140418570-G-T

2369364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140418586-G-T

http://identifiers.org/hco/7/GRCh38#2369366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140418588-C-A

2369366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140418588-C-T

http://identifiers.org/hco/7/GRCh38#2369369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140418591-C-A

2369377-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140418599-T-A

2369377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140418599-T-C

http://identifiers.org/hco/7/GRCh38#2369393-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140418614-A-C

2369393-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140418614-A-T

http://identifiers.org/hco/7/GRCh38#2369418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140418635-C-A

2369418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140418635-C-T

2369442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140418653-G-A

2369508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 140418715-C-T

2371739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140421968-G-A

2372522-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: 140422904-T-A

2372522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: 140422904-T-C

2372523-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: 140422905-T-A

2372523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: 140422905-T-C

2372527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: 140422909-G-T

http://identifiers.org/hco/7/GRCh38#2372540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140422927-C-A

2372540-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: 140422927-C-G

2372540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: 140422927-C-T

http://identifiers.org/hco/7/GRCh38#2372553-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140422937-A-C

2372553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: 140422937-A-G

2372553-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: 140422937-A-T

2372575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: 140422948-G-A

2372575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: 140422948-G-T

http://identifiers.org/hco/7/GRCh38#2372582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140422955-C-A

2372582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: 140422955-C-G

2372592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: 140422965-G-T

2372807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: 140423174-G-A

2372807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron variant
orthologous variants: 140423174-G-T

2374469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 140424007-G-A

2374469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 140424007-G-T

2374484-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 140424027-T-G

2374492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 140424035-C-T

2374617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 140424165-G-A

2374629-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 140424177-T-A

2375512-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 140425791-C-G

2376122-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140426133-T-A

2376970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 140426761-G-A

2376970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 140426761-G-T

http://identifiers.org/hco/7/GRCh38#2377169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140426957-C-A

2377169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140426957-C-T

http://identifiers.org/hco/7/GRCh38#2377188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140426976-C-A

2377188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140426976-C-T

http://identifiers.org/hco/7/GRCh38#2378565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140427372-C-A

2378565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140427372-C-T

2378700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 140427503-G-A

2378700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 140427503-G-T

2378921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140427632-G-A

2378921-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140427632-G-C

2378921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140427632-G-T

2378939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140427650-G-A

2378939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140427650-G-T

2379084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140427826-G-A

2379113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140427862-T-C

2379191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 140427936-G-A

2379191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 140427936-G-T

2379288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140427997-C-T

2379303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140428008-G-A

2379303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140428008-G-T

http://identifiers.org/hco/7/GRCh38#2379328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140428031-C-A

2379328-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140428031-C-G

2379328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140428031-C-T

2379368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140428051-G-A

2379470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 140428151-A-G

http://identifiers.org/hco/7/GRCh38#2379499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140428180-C-A

2379499-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 140428180-C-G

2379501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 140428181-G-A

2379501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 140428181-G-T

2379585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140428206-G-A

2379585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140428206-G-T

http://identifiers.org/hco/7/GRCh38#2379591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140428212-C-A

2379591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140428212-C-T

http://identifiers.org/hco/7/GRCh38#2379689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140428241-C-A

2379689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140428241-C-T

2379717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140428268-T-C

2379722-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140428273-C-G

2379722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140428273-C-T

http://identifiers.org/hco/7/GRCh38#2379794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140428334-C-A

2379794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140428334-C-T

2379795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140428335-A-G

2379805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140428345-A-G

2379829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140428368-C-T

2379834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140428373-G-A

2379834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140428373-G-T

2379910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140428409-T-C

2379910-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140428409-T-G

2379952-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140428425-T-A

2379952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140428425-T-C

2379960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140428433-G-A

2379960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140428433-G-T

2379980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140428453-G-T

2380010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140428467-G-A

2380010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140428467-G-T

2380098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140428522-G-A

2380098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140428522-G-T

2380163-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140428548-T-A

2380163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140428548-T-C

http://identifiers.org/hco/7/GRCh38#2380196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140428559-C-A

2380196-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 140428559-C-G

2380196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 140428559-C-T

http://identifiers.org/hco/7/GRCh38#2380212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140428573-C-A

http://identifiers.org/hco/7/GRCh38#2380267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#140428617-C-A

2380267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140428617-C-T

2380285-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 140428635-C-G

2380285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 140428635-C-T

2380326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 140428679-G-A

2380387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 140428738-C-T

2380460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 140428807-C-T

2380718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 140429092-G-A

2380718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3280
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 140429092-G-T