244452159-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 177624291-C-G

244452159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 177624291-C-T

244452237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 177624362-C-T

244452252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 177624378-G-A

244452515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177624631-G-A

http://identifiers.org/hco/1/GRCh38#244461244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177635968-C-A

244461244-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177635968-C-G

244461244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177635968-C-T

244461265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 177635989-G-A

244461265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 177635989-G-T

244461317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 177636041-G-A

244461317-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 177636041-G-C

244461317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 177636041-G-T

http://identifiers.org/hco/1/GRCh38#244461323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177636047-C-A

244461323-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 177636047-C-G

244461323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 177636047-C-T

244461346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 177636068-G-A

244461346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 177636068-G-T

244461355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 177636077-G-A

244461355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 177636077-G-T

244461399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 177636085-G-A

244461399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained, undefined
orthologous variants: 177636085-G-T

244461421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 177636107-G-A

244461421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 177636107-G-C

244461421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 177636107-G-T

http://identifiers.org/hco/1/GRCh38#244461429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#177636115-C-A

244461429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 177636115-C-G

244461429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 177636115-C-T

244461440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 177636126-G-A

244461440-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 177636126-G-C

244461440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 177636126-G-T

244461441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 177636130-G-A

244461441-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 177636130-G-C

244461441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained, synonymous_variant, undefined
orthologous variants: 177636130-G-T

http://identifiers.org/hco/1/GRCh38#244461449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177636138-C-A

244461449-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 177636138-C-G

244461449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 177636138-C-T

244461453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 177636142-G-A

244461453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 177636142-G-T

http://identifiers.org/hco/1/GRCh38#244461466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177636155-C-A

244461466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 177636155-C-T

244461536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 177819162-T-C

244461536-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 177819162-T-G

http://identifiers.org/hco/1/GRCh38#244461577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#177819172-C-A

244461577-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 177819172-C-G

244461577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 177819172-C-T

244461593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 177819188-G-A

244461593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 177819188-G-C

244461593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 177819188-G-T

244461595-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 177819190-T-A

244461595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 177819190-T-C

244461595-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 177819190-T-G

244461618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177819210-G-A

244461618-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177819210-G-C

244461618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177819210-G-T

244461621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177819213-T-C

244461621-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177819213-T-G

244461767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 177819327-C-T

244462266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177826392-C-T

244462432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177643108-C-T

244462567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177643572-A-G

244462637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177643669-A-G

244462656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177643688-A-G

244462969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177646065-G-A

244463675-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177647026-T-A

244463675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177647026-T-C

244463675-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177647026-T-G

244463676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177647027-A-G

244463699-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177647055-T-A

244463702-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177647058-G-C

244463706-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177647061-C-G

244463752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177647106-T-C

244463773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177647140-G-T

244463783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177647151-A-G

244463783-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177647151-A-T

244463784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177647152-G-T

244463847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177647200-A-G

244463882-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177647236-T-A

http://identifiers.org/hco/1/GRCh38#244463894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177647248-C-A

244463894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177647248-C-T

http://identifiers.org/hco/1/GRCh38#244463899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177647253-C-A

244463899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177647253-C-T

244463952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 177647309-G-T

http://identifiers.org/hco/1/GRCh38#244463974-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177647333-A-C

244463974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177647333-A-G

244463990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177647337-A-G

244464059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177647394-T-C

244464083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177647422-G-A

244464083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177647422-G-T

244464143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177647481-A-G

244464270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177648020-A-G

244464276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177648026-A-G

http://identifiers.org/hco/1/GRCh38#244464333-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177648069-A-C

244464368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177648109-A-G

244464384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177648157-T-C

http://identifiers.org/hco/1/GRCh38#244464459-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177648441-A-C

244464473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177648455-T-C

244464503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177648485-C-T

244464697-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177648677-A-T

244477422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177652765-G-T

http://identifiers.org/hco/1/GRCh38#244477456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177652799-C-A

244477477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177652819-A-G

244477525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177652869-T-C

244477526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177652870-T-C

244477527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177652871-G-A

244477527-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177652871-G-C

244477582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 177652926-T-C

244477630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177652993-T-C

http://identifiers.org/hco/1/GRCh38#244477666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177653035-C-A

244477667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177653036-A-G

244477674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177653043-G-A

244477718-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177653073-T-G

http://identifiers.org/hco/1/GRCh38#244477719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177653074-C-A

244477746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177653101-A-G

http://identifiers.org/hco/1/GRCh38#244477801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177653596-C-A

244477801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177653596-C-T

244477826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177653621-T-C

244477829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177653624-G-A

244477849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177653644-A-G

244477854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177653650-A-G

244477877-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177653673-T-G

http://identifiers.org/hco/1/GRCh38#244477900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177653701-C-A

244477966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 177653767-T-C

244477967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 177653768-A-G

244477987-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177653789-T-A

244478022-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177653837-G-C

244478066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177653922-A-G

244478066-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177653922-A-T

244478090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177653942-G-T

244478098-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177653950-T-A

244478100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177653952-T-C

244478105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177653957-T-C

244478147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177653998-A-G

244478152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177653999-T-C

244478172-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177654017-A-T

244479602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177656135-G-A

http://identifiers.org/hco/1/GRCh38#244479606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177656139-C-A

244479618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177656147-G-T

244479633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177656159-T-C

244479641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177656167-G-A

244479641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177656167-G-T

244479657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177656183-T-C

http://identifiers.org/hco/1/GRCh38#244479659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177656185-C-A

244479659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177656185-C-T

http://identifiers.org/hco/1/GRCh38#244479693-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177656214-A-C

244479804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177656329-A-G

244479856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177656385-A-G

244479883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177656414-A-G

http://identifiers.org/hco/1/GRCh38#244479899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177656431-C-A

244479899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177656431-C-T

http://identifiers.org/hco/1/GRCh38#244479915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177656447-C-A

http://identifiers.org/hco/1/GRCh38#244479926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177656458-C-A

244479926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177656458-C-T

244480639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177665490-G-A

244480656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177665506-C-T

244481599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177665796-A-G

244481786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177665959-T-C

244490375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177670339-T-C

244490421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177670385-A-G

244490449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 177670413-A-G

244490489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177670448-T-C

244490518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177670477-T-C

244490537-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177670495-T-A

244490537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177670495-T-C

244490568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177670520-T-C

244490582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177670543-A-G

244490582-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177670543-A-T

http://identifiers.org/hco/1/GRCh38#244490619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177670589-C-A

244490619-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177670589-C-G

244490619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177670589-C-T

244490626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177670601-T-C

244490653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177670618-C-T

244490661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177670626-C-T

http://identifiers.org/hco/1/GRCh38#244490677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177670637-C-A

244490757-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177670697-T-A

244490767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177670703-T-C

244490850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177670762-C-T

244490892-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177670797-A-T

244499126-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177677916-T-A

244499126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177677916-T-C

244499165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177677956-A-G

http://identifiers.org/hco/1/GRCh38#244499227-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177678018-A-C

244499227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177678018-A-G

http://identifiers.org/hco/1/GRCh38#244501448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177678291-C-A

244501485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177678326-G-A

244504076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177678669-A-G

244504102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177678695-C-T

244504248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177678808-T-C

244504255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177678815-A-G

244504442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177678961-G-T

244505070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177679524-A-G

244505123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177679575-C-T

244518447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177684835-A-G

244518487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177684875-A-G

244518507-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177684895-T-A

244518545-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177684943-T-G

244518574-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177684972-T-A

244518574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177684972-T-C

244518581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177684979-T-C

244518599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 177685003-T-C

244518627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 177685031-G-A

244518627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 177685031-G-T

244518651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 177685055-A-G

244518727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177685133-A-G

244518735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177685141-G-A

244518735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177685141-G-T

244518742-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177685148-T-A

244518742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177685148-T-C

244518742-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177685148-T-G

244518779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177685185-A-G

244518782-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177685188-T-A

244518782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177685188-T-C

http://identifiers.org/hco/1/GRCh38#244518785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177685191-C-A

244518785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177685191-C-T

244518920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177685346-A-G

244518987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177685401-A-G

http://identifiers.org/hco/1/GRCh38#244610490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177776005-C-A

244610490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 177776005-C-T

244610539-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 177776053-T-A

244610539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 177776053-T-C

244610539-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 177776053-T-G

244610604-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177776116-T-A

244610604-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177776116-T-G

244610605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177776117-G-A

244610605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177776117-G-T

244611676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177776539-C-T

244611805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177776641-A-G

244611815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177776647-G-A

244611821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177776653-G-A

http://identifiers.org/hco/1/GRCh38#244611842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177776666-C-A

244611888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177776712-T-C

244611903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28491
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177776727-C-T