http://identifiers.org/hco/2/GRCh38#101397503-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39704600-A-C

101397557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 39704650-A-G

101397771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39704899-A-G

101398553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39705181-G-A

101398557-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39705185-G-C

101398798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39705445-C-T

101399078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39705850-G-A

101399208-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39705982-C-G

101399268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39706041-G-A

101399293-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39706086-G-C

101399576-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39706364-T-A

101399780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39706517-G-A

101399780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39706517-G-T

101400040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39706730-G-T

101400091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39706780-C-T

101400527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39707160-G-A

101400527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39707160-G-T

101400534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39707167-T-C

101400603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39707212-T-C

101400604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39707213-G-A

101400697-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39707300-T-A

101400697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39707300-T-C

101402445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 39709439-C-T

101402495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 39709489-C-T

101402704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 39709695-A-G

101402751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, splice_region_variant, synonymous_variant
orthologous variants: 39709742-G-T

101402783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39709773-C-T

http://identifiers.org/hco/2/GRCh38#101402805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39709794-C-A

101402805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39709794-C-G

101402805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39709794-C-T

101402826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39709825-A-G

101402872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39709872-C-G

101405566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39710889-A-G

101405710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39711033-C-T

101405800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39711088-G-A

101405885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39711170-G-T

101406037-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 39711440-C-G

101406037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 39711440-C-T

101406075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39711482-G-A

101406075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39711482-G-T

http://identifiers.org/hco/2/GRCh38#101406103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39711510-C-A

101406105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39711512-A-G

http://identifiers.org/hco/2/GRCh38#101406107-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39711514-A-C

101406107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39711514-A-G

101406127-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39711537-T-A

101406177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39711590-G-A

101406177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39711590-G-T

101406179-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39711592-T-A

101406179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39711592-T-C

101406249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39712991-G-A

101406260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39713002-G-C

101406281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39713023-G-A

101406281-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39713023-G-C

101407848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39715564-C-T

101407898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39715643-C-T

101408094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39715836-G-A

http://identifiers.org/hco/2/GRCh38#101409789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39716544-C-A

101409789-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39716544-C-G

101409789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39716544-C-T

101409885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39716648-A-G

101409892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39716655-G-A

http://identifiers.org/hco/2/GRCh38#101410174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39717269-C-A

101410174-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39717269-C-G

101410236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39717332-C-T

101410299-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39717391-T-A

101410299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39717391-T-C

101410373-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39717456-C-G

http://identifiers.org/hco/2/GRCh38#101410585-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#39717782-A-C

101410585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 39717782-A-G

101410745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39717942-T-C

101410816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39718003-A-G

101410816-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39718003-A-T

101410817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39718004-G-T

http://identifiers.org/hco/2/GRCh38#101410827-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39718014-A-C

http://identifiers.org/hco/2/GRCh38#101410833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39718020-C-A

101411135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39718292-C-T

101411182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39718358-A-G

101411434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39718564-A-G

http://identifiers.org/hco/2/GRCh38#101411603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39718718-C-A

101411812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39718870-G-A

101411907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39718959-G-A

101412005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39719031-C-T

101412160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39719120-G-A

101412206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39719136-C-T

101412293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39719196-C-T

101412294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39719197-G-A

101412469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39719365-T-C

101412541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39719435-G-T

http://identifiers.org/hco/2/GRCh38#101412638-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39719543-A-C

101412641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39719546-A-G

101412682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39719591-A-G

101412682-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39719591-A-T

101412778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39719711-A-G

101412781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39719714-G-A

101412781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39719714-G-T

101412785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39719717-G-T

http://identifiers.org/hco/2/GRCh38#101412824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39719860-C-A

101412825-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39719861-T-A

101412825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39719861-T-C

101412940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 39720027-T-C

101412955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 39720042-C-T

101413024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 39720111-C-T

101413069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, splice_region_variant, synonymous_variant
orthologous variants: 39720156-A-G

http://identifiers.org/hco/2/GRCh38#101413127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39720209-C-A

101413127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39720209-C-T

101413174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39720259-A-G

101413421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39720532-G-A

101413421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39720532-G-C

101413465-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39720567-T-A

101413478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39720580-C-T

101413709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39720789-G-A

101413710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39720790-C-T

101414560-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39721835-C-G

101414560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39721835-C-T

101414608-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39721882-C-G

101414608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39721882-C-T

101414618-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39721895-G-C

101414618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39721895-G-T

http://identifiers.org/hco/2/GRCh38#101414809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39722041-C-A

101414809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39722041-C-T

101414842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39722057-G-A

101414842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39722057-G-T

http://identifiers.org/hco/2/GRCh38#101414978-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39722194-A-C

101414978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39722194-A-G

http://identifiers.org/hco/2/GRCh38#101415007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39722218-C-A

101415007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39722218-C-T

101415010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39722221-A-G

http://identifiers.org/hco/2/GRCh38#101415030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39722247-C-A

101415030-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39722247-C-G

101415030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39722247-C-T

http://identifiers.org/hco/2/GRCh38#101415038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39722255-C-A

101415038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39722255-C-T

http://identifiers.org/hco/2/GRCh38#101415045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39722262-C-A

101415045-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39722262-C-G

101415045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39722262-C-T

101415049-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39722266-T-A

101415049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39722266-T-C

101415050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39722267-G-A

101415050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39722267-G-T

http://identifiers.org/hco/2/GRCh38#101415056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39722274-C-A

101415056-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39722274-C-G

101415056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39722274-C-T

101415057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39722275-T-C

101415057-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39722275-T-G

101415104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39722322-C-T

101415253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39722466-C-T

101415254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39722467-C-T

101415262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39722475-C-T

101415289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39722516-C-T

101415360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39722584-C-T

http://identifiers.org/hco/2/GRCh38#101415377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39722600-C-A

http://identifiers.org/hco/2/GRCh38#101417555-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39722781-A-C

http://identifiers.org/hco/2/GRCh38#101417692-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39722918-A-C

101417692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 39722918-A-G

101417697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39722923-T-C

http://identifiers.org/hco/2/GRCh38#101417700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39722926-C-A

101417700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39722926-C-T

101417728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39722948-A-G

101417741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39722958-G-A

101417741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39722958-G-T

101417750-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39722970-T-G

101417772-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39722992-T-A

101417829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39723029-G-T

101418839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39724643-G-A

101418839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39724643-G-T

101418857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 39724661-C-T

101418980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39724780-G-T

101418996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39724797-C-T

101419015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39724816-G-A

101419015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39724816-G-T

101419021-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39724822-C-G

101419021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39724822-C-T

http://identifiers.org/hco/2/GRCh38#101419024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39724825-C-A

101419347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39725319-C-T

101419401-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39725384-G-C

101421104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39726898-T-C

101421120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39726914-G-T

101421166-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39726956-A-T

http://identifiers.org/hco/2/GRCh38#101421282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39727355-C-A

http://identifiers.org/hco/2/GRCh38#101421349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39727422-C-A

101421464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 39727507-G-A

101421474-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 39727517-T-G

101421532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 39727575-T-C

http://identifiers.org/hco/2/GRCh38#101421546-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39727587-A-C

101421576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 39727620-G-A

101421663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 39727696-A-G

101421668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 39727701-T-C

101421751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 39727784-G-A

http://identifiers.org/hco/2/GRCh38#101421865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39727895-C-A

101421997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39728019-C-T

101422023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39728048-C-T

101422137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39729041-G-A

101422216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39729128-G-T

101422265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39729176-G-T

http://identifiers.org/hco/2/GRCh38#101422269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39729180-C-A

http://identifiers.org/hco/2/GRCh38#101422275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39729181-C-A

101422295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39729200-G-A

101422441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 39729330-G-A

http://identifiers.org/hco/2/GRCh38#101422648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39729511-C-A

101423866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39730550-C-T

101424040-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39730668-G-C

101424048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39730676-G-A

101426727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39732499-A-G

101426922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39732669-T-C

http://identifiers.org/hco/2/GRCh38#101427038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39732756-C-A

101427038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39732756-C-T

101427117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39732833-G-A

101427173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39732870-A-G

101427427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39733058-G-T

101427574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39733191-C-T

101427590-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39733207-C-G

101427590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39733207-C-T

101428524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39734677-C-T

101428666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39734820-A-G

101428739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39734891-G-A

101428743-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39734895-A-T

101428809-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39734953-T-G

101428810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39734954-G-A

101428810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39734954-G-T

101428820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39734964-G-T

http://identifiers.org/hco/2/GRCh38#101428834-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39734984-A-C

101428834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39734984-A-G

101428834-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39734984-A-T

101428897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39735009-A-G

http://identifiers.org/hco/2/GRCh38#101428902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39735014-C-A

101428902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39735014-C-T

101428921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39735027-G-A

101428921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39735027-G-T

101428923-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39735029-C-G

http://identifiers.org/hco/2/GRCh38#101429001-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39735103-A-C

101429001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 39735103-A-G

101429028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39735130-G-A

101429028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39735130-G-T

http://identifiers.org/hco/2/GRCh38#101429048-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39735150-A-C

101429070-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39735172-T-G

101429071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39735173-G-T

101429076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39735178-G-A

101429076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39735178-G-T

http://identifiers.org/hco/2/GRCh38#101429136-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39735238-A-C

101429136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39735238-A-G

101429186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39735291-C-T

101429270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39735377-C-T

101429358-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39735463-T-A

101429373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39735478-T-C

101429439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39735545-A-G

101429635-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39735672-T-A

101429641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39735678-T-C

101429749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39735774-T-C

http://identifiers.org/hco/2/GRCh38#101429815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39735814-C-A

101429815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39735814-C-T

http://identifiers.org/hco/2/GRCh38#101429871-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39735844-A-C

101430013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39735958-A-G

101430218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39736145-G-A

101431029-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39736914-A-T

101431218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39737179-G-A

101432601-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39737733-C-G

101432601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39737733-C-T

http://identifiers.org/hco/2/GRCh38#101432638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39737770-C-A

101432638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39737770-C-T

101432763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39737894-T-C

101432793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39737911-C-T

101432862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39737964-C-T

101432893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 39737988-A-G

101433047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39738120-G-T

101433471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39738635-G-A

101433588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39738762-A-G

101433781-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39738950-G-C

101434464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39739901-A-G

http://identifiers.org/hco/2/GRCh38#101434565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39740000-C-A

101434565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39740000-C-T

101434734-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39740204-A-T

http://identifiers.org/hco/2/GRCh38#101434735-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39740205-A-C

101434758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39740227-T-C

101434762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39740231-A-G

101434762-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39740231-A-T

101434781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39740250-A-G

101434868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 39740320-G-A

101434868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 39740320-G-T

http://identifiers.org/hco/2/GRCh38#101435001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39740450-C-A

101435035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 39740473-G-A

http://identifiers.org/hco/2/GRCh38#101435098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39740542-C-A

101435098-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 39740542-C-G

101435131-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 39740580-G-C

101435131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 39740580-G-T

http://identifiers.org/hco/2/GRCh38#101435160-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#39740607-A-C

101435160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 39740607-A-G

101435160-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 39740607-A-T

101435161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 39740608-G-T

http://identifiers.org/hco/2/GRCh38#101435243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#39740698-C-A

http://identifiers.org/hco/2/GRCh38#101435364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#39740990-C-A

101435551-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 39741137-T-A

101435551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 39741137-T-C

http://identifiers.org/hco/2/GRCh38#101435698-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#39741249-A-C

101436065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39741563-G-A

101436068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39741566-C-T

http://identifiers.org/hco/2/GRCh38#101436094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39741585-C-A

101436094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39741585-C-T

101436104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39741595-G-A

101436341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39741807-T-C

http://identifiers.org/hco/2/GRCh38#101436519-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39742037-A-C

101436600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39742111-G-A

101436704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39742207-G-T

101436911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39742363-G-A

101437014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39742436-G-A

101448002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39746911-C-T

101448040-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39746949-A-T

101448055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39746970-G-T

101448240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39747185-C-T

101448548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39747469-C-T

101448603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39747503-T-C

101448683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39747580-G-T

101448779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39747655-C-T

101448810-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39747685-A-T

101449482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39748669-A-G

101449499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39748686-G-A

101449499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39748686-G-T

101449680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39748828-G-A

101449728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39748878-A-G

101449792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39748944-A-G

101449813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39748965-G-A

101450098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39749163-G-A

101450529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39749257-G-T

101450555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39749282-G-A

101450555-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39749282-G-C

101450555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39749282-G-T

http://identifiers.org/hco/2/GRCh38#101450602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39749326-C-A

101450602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 39749326-C-T

101450668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 39749392-A-G

101450690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39749412-T-C

101450699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39749421-T-C

101450706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39749428-A-G

101451000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39749820-C-T

http://identifiers.org/hco/2/GRCh38#101451013-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39749833-A-C

101451161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39749917-C-T

101451331-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39750085-T-G

101452231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39750385-T-C

http://identifiers.org/hco/2/GRCh38#101452238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39750393-C-A

101452238-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39750393-C-G

101452238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39750393-C-T

101452242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39750397-G-A

101452242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39750397-G-T

101452309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39750463-T-C

101452309-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39750463-T-G

101453742-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39751131-C-G

101453880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39751280-A-G

101463292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39752172-G-A

101463398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39752304-G-A

101463491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39752382-G-A

101463525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39752412-C-T

101463755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39752603-C-T

101463780-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39752628-G-C

101463799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39752645-G-A

101463803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39752649-G-C

101463813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39752659-G-T

101463821-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39752667-G-C

http://identifiers.org/hco/2/GRCh38#101464056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39753048-C-A

101464143-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39753119-G-C

101464248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39753221-A-G

101464275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39753248-G-A

101464309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39753282-T-C

101464424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39753372-G-A

101464427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39753376-A-G

101464684-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39753631-T-G

101464742-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39753682-T-G

101464928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39753977-T-C

101464936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39753985-G-T

101465018-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39754067-T-G

101465082-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39754130-G-C

101465109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39754159-T-C

101465123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39754173-A-G

101465795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39754385-C-T

101465810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39754411-G-T

101465841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39754441-A-G

101466097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39754693-T-C

http://identifiers.org/hco/2/GRCh38#101466671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39757310-C-A

101466745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39757547-G-A

101466745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39757547-G-T

101466759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39757561-T-C

101466944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39757751-T-C

101466947-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39757756-T-A

101466948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39757757-A-G

http://identifiers.org/hco/2/GRCh38#101466971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39757781-C-A

http://identifiers.org/hco/2/GRCh38#101466972-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39757782-A-C

101467004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39757811-T-C

http://identifiers.org/hco/2/GRCh38#101467009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39757817-C-A

101467009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39757817-C-T

101467097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39757902-T-C

101470350-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39758514-C-G

101470359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39758522-G-A

101470469-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39758625-T-G

101470479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39758633-A-G

101473178-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39759170-T-A

101473654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39759547-T-C

101473840-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39759740-G-C

101473986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39759885-C-T

101474044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39759938-G-A

101474076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39759959-G-A

101474081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39759964-G-A

101474081-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39759964-G-C

http://identifiers.org/hco/2/GRCh38#101474085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39759967-C-A

101474085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39759967-C-T

http://identifiers.org/hco/2/GRCh38#101474110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#39759979-C-A

101474110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 39759979-C-T

101474111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 39759980-G-A

101474111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 39759980-G-T

101474120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 39759989-A-G

http://identifiers.org/hco/2/GRCh38#101474155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39760000-C-A

101474155-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39760000-C-G

101474155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39760000-C-T

101474176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39760021-A-G

http://identifiers.org/hco/2/GRCh38#101474246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39760073-C-A

101474246-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 39760073-C-G

101474246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 39760073-C-T

101474384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39760163-A-G

101474384-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39760163-A-T

101474390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 39760169-G-A

101474390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 39760169-G-T

101474394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 39760173-G-A

101474394-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 39760173-G-C

101474394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 39760173-G-T

101474408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 39760195-G-A

101474408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 39760195-G-T

101474427-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 39760214-T-G

101474433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 39760219-A-G

101474449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39760235-G-A

http://identifiers.org/hco/2/GRCh38#101474526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39760306-C-A

101474540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39760320-G-A

http://identifiers.org/hco/2/GRCh38#101474563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39760329-C-A

101474563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39760329-C-T

http://identifiers.org/hco/2/GRCh38#101474586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39760341-C-A

101474586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39760341-C-T

http://identifiers.org/hco/2/GRCh38#101474607-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39760362-A-C

101474607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39760362-A-G

101474607-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39760362-A-T

http://identifiers.org/hco/2/GRCh38#101474614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39760369-C-A

101474614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39760369-C-T

http://identifiers.org/hco/2/GRCh38#101474629-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39760383-A-C

101474629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 39760383-A-G

http://identifiers.org/hco/2/GRCh38#101474631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39760385-C-A

http://identifiers.org/hco/2/GRCh38#101474636-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, splice_donor_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39760390-A-C

101474649-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 39760404-T-A

101474649-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 39760404-T-G

101474668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 39760423-G-A

101474668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 39760423-G-T

http://identifiers.org/hco/2/GRCh38#101474730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39760491-C-A

http://identifiers.org/hco/2/GRCh38#101474731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#39760492-C-A

101474731-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 39760492-C-G

101474731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 39760492-C-T

101474732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 39760493-C-T

101474803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: 5 prime UTR variant
orthologous variants: 39760543-G-C

101474803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: 5 prime UTR variant
orthologous variants: 39760543-G-T

101474961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: 5 prime UTR variant
orthologous variants: 39760652-G-T

101474967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37253
most severe consequence: 5 prime UTR variant
orthologous variants: 39760658-T-C