6808738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18981349-T-C

6808805-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18981423-T-G

6808806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18981424-T-C

6808892-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18981539-C-G

6808892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18981539-C-T

http://identifiers.org/hco/8/GRCh38#6808895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18981542-C-A

6808895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18981542-C-T

6808905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18981552-T-C

6808926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18981562-T-C

http://identifiers.org/hco/8/GRCh38#6808993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18981626-C-A

6808993-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18981626-C-G

6809012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18981674-G-A

6809088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18981784-T-C

6809088-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18981784-T-G

6809118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18981814-G-A

6809118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18981814-G-T

6809187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18981880-G-A

6809187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18981880-G-T

http://identifiers.org/hco/8/GRCh38#6809217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18981913-C-A

6809217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18981913-C-T

6809218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18981914-G-A

6809218-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18981914-G-C

6809250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18981948-G-A

6809250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18981948-G-T

6809290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18981986-A-G

6810354-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18982393-A-T

http://identifiers.org/hco/8/GRCh38#6810358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18982397-C-A

6810358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18982397-C-G

6810360-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18982399-T-G

6810787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18983114-A-G

6810827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18983154-G-T

6810828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18983155-T-C

6810829-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18983156-A-T

6810922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18983243-A-G

6810945-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18983252-A-T

6810975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18983299-T-C

6810975-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18983299-T-G

6810980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18983309-G-A

6810980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18983309-G-C

6810980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18983309-G-T

6810981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18983310-A-G

6810981-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18983310-A-T

http://identifiers.org/hco/8/GRCh38#6810994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18983323-C-A

6810994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18983323-C-T

6811003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18983332-G-T

6811008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18983334-G-A

6811008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18983334-G-T

6811009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18983335-T-C

6811009-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18983335-T-G

6811054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18983379-A-G

6811123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18983435-G-A

6811123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18983435-G-T

6811196-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18983508-G-C

6811196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 18983508-G-T

6811246-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 18983558-G-C

6811246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 18983558-G-T

http://identifiers.org/hco/8/GRCh38#6811427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18983727-C-A

http://identifiers.org/hco/8/GRCh38#6811474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18983762-C-A

6811483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 18983771-G-A

6811483-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 18983771-G-C

6811483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 18983771-G-T

6811511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 18983796-G-A

6811516-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 18983801-T-A

6811516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 18983801-T-C

6811516-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 18983801-T-G

http://identifiers.org/hco/8/GRCh38#6811553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18983835-C-A

6811553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 18983835-C-T

6811556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 18983838-G-T

6811568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 18983850-T-C

6811568-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 18983850-T-G

6811681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 18983960-C-T

6811783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 18984062-G-A

6811783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 18984062-G-T

6811881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 18984160-G-A

6811881-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 18984160-G-C

6811881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 18984160-G-T

6812010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 18984292-C-T

http://identifiers.org/hco/8/GRCh38#6812083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18984365-C-A

6812092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 18984374-C-T

6812106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 18984388-G-A

6812106-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 18984388-G-C

6812108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 18984390-G-A

6812110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 18984392-G-A

6812110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 18984392-G-C

6812110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 18984392-G-T

6812122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 18984404-G-A

6812122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 18984404-G-T

6812130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 18984412-G-A

6812130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 18984412-G-T

6812170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 18984452-T-C

http://identifiers.org/hco/8/GRCh38#6812189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18984471-C-A

6812189-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 18984471-C-G

6812235-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 18984517-T-A

6812235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 18984517-T-C

6812235-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 18984517-T-G

6812275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 18984557-G-A

6812275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 18984557-G-T

6812288-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 18984570-T-A

6812288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 18984570-T-C

http://identifiers.org/hco/8/GRCh38#6812474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18984764-C-A

6812474-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18984764-C-G

6812486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18984776-A-G

6812486-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18984776-A-T

6812570-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18984859-C-G

http://identifiers.org/hco/8/GRCh38#6812822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18985068-C-A

http://identifiers.org/hco/8/GRCh38#6813120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18985379-C-A

6813271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18985506-G-T

6815801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18987237-A-G

http://identifiers.org/hco/8/GRCh38#6815829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18987265-C-A

6815829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 18987265-C-T

6815921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 18987357-G-A

6815921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 18987357-G-T

6816020-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18987422-A-T

6816052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18987451-G-A

6816052-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18987451-G-C

6816052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18987451-G-T

6816086-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18987487-T-A

6821829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18989037-A-G

6821871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, splice_region_variant
orthologous variants: 18989086-T-C

6821926-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 18989141-G-C

6821976-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 18989191-T-G

6822004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 18989219-G-A

6822004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 18989219-G-C

6822004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 18989219-G-T

6822083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18989296-T-C

6822155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18989300-A-G

6822254-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18989396-G-C

http://identifiers.org/hco/8/GRCh38#6822330-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18989474-A-C

6822343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18989487-T-C

6822359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18989503-T-C

6822377-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18989517-A-T

6822427-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18989567-C-G

6822429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18989569-C-G

6822429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18989569-C-T

6822755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18989901-A-G

6822766-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18989912-C-G

http://identifiers.org/hco/8/GRCh38#6822800-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18989936-A-C

6822923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18990050-A-G

6822933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18990060-T-C

6822959-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18990077-G-C

6823140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18990261-C-T

6823178-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18990298-C-G

6823246-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18990365-C-G

6823246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18990365-C-T

6823554-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, stop_gained
orthologous variants: 18990662-T-A

6823648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 18990756-G-A

6823669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 18990777-G-A

6823669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 18990777-G-T

http://identifiers.org/hco/8/GRCh38#6823673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18990781-C-A

6823673-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 18990781-C-G

6823673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 18990781-C-T

6823739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18990848-G-A

6823739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18990848-G-T

6823801-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18990897-T-A

6823801-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18990897-T-G

6823806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18990902-G-A

6823806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18990902-G-T

6823855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18990951-G-A

6823855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18990951-G-T

6823857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18990953-G-A

6823857-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18990953-G-C

http://identifiers.org/hco/8/GRCh38#6823916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18991008-C-A

6823916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18991008-C-T

6824012-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18991082-C-G

6824298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18991303-G-T

6824366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18991410-G-A

6824435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18991487-G-A

6824874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18991664-T-C

6824874-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18991664-T-G

6825047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18991833-G-A

6825047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18991833-G-T

http://identifiers.org/hco/8/GRCh38#6825051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18991837-C-A

6825051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18991837-C-T

6825090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18991880-T-C

6825117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18991913-C-T

6825124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18991922-G-A

6825124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18991922-G-T

6825125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18991923-G-A

6825125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18991923-G-T

6825184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 18991980-G-A

6825184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 18991980-G-T

6825265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 18992061-C-T

6825329-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 18992125-G-C

6825364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18992159-A-G

6825373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18992168-G-A

6825373-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18992168-G-C

6825373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18992168-G-T

6825394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18992189-G-A

6825394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18992189-G-T

http://identifiers.org/hco/8/GRCh38#6825407-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18992205-A-C

6825407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18992205-A-G

6825504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18992304-T-C

6825600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18992376-C-T

6825883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18992651-C-T

6825894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18992662-C-T

6825900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18992668-G-A

http://identifiers.org/hco/8/GRCh38#6825903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18992671-C-A

6825908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18992676-G-A

6825938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18992706-G-A

6825970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18992738-G-A

6825976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18992744-C-T

6825984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18992752-G-T

6826050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18992822-A-G

6826152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18992892-T-C

6826152-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18992892-T-G

6826250-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18992987-T-A

6826250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18992987-T-C

6826330-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18993070-A-T

6826334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18993074-T-C

6826334-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18993074-T-G

6826336-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18993076-T-A

6826456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18993216-G-A

6826480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18993240-G-A

6826482-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18993243-T-A

6826570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18993311-G-T

6826579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18993324-G-A

6826648-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18993400-G-C

6826910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18993803-C-T

6826985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18993875-G-A

6827005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18993890-A-G

6827053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18993946-G-A

6827062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18993955-A-G

6827062-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18993955-A-T

6827134-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18994012-G-C

6829098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18995605-G-C

http://identifiers.org/hco/8/GRCh38#6829099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18995606-C-A

6829099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18995606-C-T

6829131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18995634-A-G

6829137-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18995640-C-G

http://identifiers.org/hco/8/GRCh38#6829229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18995713-C-A

6829271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 18995760-G-T

6829276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 18995765-C-G

6829298-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 18995787-A-T

6829360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18995844-T-C

6829366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18995850-A-G

6829422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18995906-T-C

http://identifiers.org/hco/8/GRCh38#6829424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18995908-C-A

6829429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18995913-G-A

6829429-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18995913-G-C

6829429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18995913-G-T

6830168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18996023-G-A

6830193-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18996056-A-T

http://identifiers.org/hco/8/GRCh38#6830225-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#18996088-A-C

6830312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18996170-G-T

6830313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 18996171-A-G

6830356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18996269-G-A

6830356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18996269-G-T

6830464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18996361-T-C

6830501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18996397-T-C

6830569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18996467-G-A

6830724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18997160-A-G

6830732-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18997168-T-A

http://identifiers.org/hco/8/GRCh38#6830824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18997226-C-A

6830825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18997227-A-G

http://identifiers.org/hco/8/GRCh38#6831034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18997398-C-A

http://identifiers.org/hco/8/GRCh38#6831121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18997487-C-A

6831121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18997487-C-T

6831658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18997901-T-C

http://identifiers.org/hco/8/GRCh38#6831670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18997913-C-A

6831670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18997913-C-T

6831674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18997917-T-C

6831683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18997925-G-A

6831683-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18997925-G-C

6831707-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18997949-A-T

http://identifiers.org/hco/8/GRCh38#6832233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18998126-C-A

6832233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18998126-C-G

6832271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18998195-C-G

6832376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18998301-G-A

6832376-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18998301-G-C

6832484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18998406-C-T

http://identifiers.org/hco/8/GRCh38#6832508-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18998430-A-C

6832521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18998443-G-A

6832521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18998443-G-T

6832577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18998477-G-A

6832577-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18998477-G-C

6832577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18998477-G-T

6832647-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18998521-T-G

6832653-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18998527-G-C

6832709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 18998567-G-A

6832709-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 18998567-G-C

6832709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 18998567-G-T

http://identifiers.org/hco/8/GRCh38#6832734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18998592-C-A

6832734-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 18998592-C-G

6832734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 18998592-C-T

6832862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 18998720-G-A

6832862-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 18998720-G-C

http://identifiers.org/hco/8/GRCh38#6832864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18998722-C-A

6832864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 18998722-C-T

6832882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 18998740-T-C

6832942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18998795-G-A

6832942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18998795-G-T

http://identifiers.org/hco/8/GRCh38#6832973-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18998820-A-C

6832973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18998820-A-G

6832995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18998838-T-C

6833070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18998876-G-A

6833100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18998906-A-G

6833115-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18998915-C-G

http://identifiers.org/hco/8/GRCh38#6833200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#18998998-C-A

6833237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18999035-C-T

6833289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18999071-G-A

6833289-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18999071-G-C

6833294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18999076-G-A

6833294-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18999076-G-C

6833294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18999076-G-T

6833370-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18999166-G-C

6833374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 18999170-T-C

6835161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 19000668-G-A

http://identifiers.org/hco/8/GRCh38#6835299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#19000752-C-A

6835299-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19000752-C-G

6835299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19000752-C-T

6835308-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19000762-C-G

6835323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19000775-G-A

6835323-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19000775-G-C

6835323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19000775-G-T

6835329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19000781-A-G

6835329-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19000781-A-T

http://identifiers.org/hco/8/GRCh38#6835507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#19000960-C-A

6835507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 19000960-C-T

http://identifiers.org/hco/8/GRCh38#6835522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#19000975-C-A

6835522-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 5 prime UTR variant
orthologous variants: 19000975-C-G

6835522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20782
most severe consequence: 5 prime UTR variant
orthologous variants: 19000975-C-T