46458949-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 76181154-T-A

46458949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 76181154-T-C

46458949-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 76181154-T-G

http://identifiers.org/hco/21/GRCh38#46458961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#76181142-C-A

46458961-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76181142-C-G

46458961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76181142-C-T

http://identifiers.org/hco/21/GRCh38#46459292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#76180877-C-A

46459292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76180877-C-T

http://identifiers.org/hco/21/GRCh38#46459313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76180859-C-A

46459313-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76180859-C-G

46459313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76180859-C-T

46459358-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76180813-T-A

46459358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76180813-T-C

46459358-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76180813-T-G

46460184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76180230-A-G

46461314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76179759-G-A

46461314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76179759-G-T

http://identifiers.org/hco/21/GRCh38#46461404-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76179683-A-C

46461636-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76179449-T-A

46462707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 76177941-G-A

46462707-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 76177941-G-C

46462707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 76177941-G-T

46462757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76177894-G-A

46462834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76177728-T-C

http://identifiers.org/hco/21/GRCh38#46462853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76177713-C-A

46462853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76177713-C-T

46462912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76177656-C-T

46462929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76177639-G-A

46462929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76177639-G-T

46483010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76167126-T-C

46483207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76166151-G-T

46483386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76165889-G-A

46483389-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76165886-T-A

http://identifiers.org/hco/21/GRCh38#46483610-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76165628-A-C

46483621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76165619-G-A

46483641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76165599-G-C

46483654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76165586-G-A

46483845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76165404-G-A

46483845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76165404-G-C

46483903-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76165297-A-T

46483988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76165220-A-G

46484081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76165117-C-T

46484135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76165068-T-C

46484185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76165020-A-G

46484714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76163646-A-G

46484721-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76163639-G-C

46484721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76163639-G-T

46484740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76163620-T-C

http://identifiers.org/hco/21/GRCh38#46484845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76163514-C-A

46484845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76163514-C-T

46484865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76163495-T-C

46488788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76159042-G-A

46489076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76158806-C-T

46489083-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76158799-A-T

46489099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76158797-G-A

46489108-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76158788-T-G

46489193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76158702-A-G

46489276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76158623-C-T

46489330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76158583-G-T

46489364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76158550-A-G

46489364-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76158550-A-T

46489686-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76158281-G-C

http://identifiers.org/hco/21/GRCh38#46489773-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76158196-A-C

46489877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76158125-C-T

46489979-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76158036-C-G

46490056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76157977-C-T

46490323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76157725-T-C

46490392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76157666-G-T

46490442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76157611-C-T

46490518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76157514-T-C

46490587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76157451-A-G

http://identifiers.org/hco/21/GRCh38#46490635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76157403-C-A

46490635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76157403-C-T

http://identifiers.org/hco/21/GRCh38#46490645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/10/GRCm39#76157393-C-A

46490645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76157393-C-T

46490756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76157273-G-A

46490756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76157273-G-T

46490772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76157259-A-G

46490782-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76157249-T-G

46490797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76157234-A-G

46490851-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76157187-T-G

46490853-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76157185-T-A

http://identifiers.org/hco/21/GRCh38#46490856-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76157182-A-C

46490856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76157182-A-G

46490856-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76157182-A-T

http://identifiers.org/hco/21/GRCh38#46496879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76155516-C-A

46496879-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76155516-C-G

46496879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76155516-C-T

46496891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76155504-T-C

46496892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76155503-T-C

http://identifiers.org/hco/21/GRCh38#46496900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76155495-C-A

46497154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76155254-A-G

http://identifiers.org/hco/21/GRCh38#46497181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76155228-C-A

46497181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76155228-C-T

46497203-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76155205-G-C

46497203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76155205-G-T

46497208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76155200-G-A

46497212-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76155196-T-A

46497212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76155196-T-C

46497259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76155149-A-G

46497287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76155121-A-G

http://identifiers.org/hco/21/GRCh38#46497406-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76155019-A-C

46497424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76155000-C-T

46497656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76154830-C-T

46497668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76154821-A-G

46498439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76154040-G-T

http://identifiers.org/hco/21/GRCh38#46498553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76153955-C-A

46498553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76153955-C-T

46498744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76153764-G-A

http://identifiers.org/hco/21/GRCh38#46498802-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76153730-A-C

46498855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76153679-C-T

http://identifiers.org/hco/21/GRCh38#46498887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76153650-C-A

46498887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76153650-C-T

46498969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76153625-G-A

46498969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76153625-G-T

46499481-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76153222-C-G

46499543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76153159-G-A

46499705-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76153048-C-G

46500046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76152786-T-C

46500214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76152648-A-G

46500388-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76152516-T-A

46500763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76151923-A-G

46500798-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76151889-G-C

46500853-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76151834-T-A

46500854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76151833-T-C

46500857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76151830-C-T

http://identifiers.org/hco/21/GRCh38#46500997-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76151700-A-C

46501216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76150976-G-A

46501284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76150912-A-G

46501759-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76150796-T-G

46501960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76150590-G-A

46502853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76150275-A-G

46503452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76149465-C-T

46504307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76149187-A-G

http://identifiers.org/hco/21/GRCh38#46504318-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76149176-A-C

46504318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76149176-A-G

http://identifiers.org/hco/21/GRCh38#46504409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/10/GRCm39#76149088-C-A

46504409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76149088-C-T

46504462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76149035-A-G

46504469-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76149028-G-C

46504480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 76149017-A-G

46504480-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 76149017-A-T

46504483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 76149014-G-A

46504524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76148973-A-G

http://identifiers.org/hco/21/GRCh38#46504556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76148945-C-A

46504556-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76148945-C-G

46504556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76148945-C-T

46504578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76148923-G-A

46504604-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76148900-A-T

http://identifiers.org/hco/21/GRCh38#46504612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76148888-C-A

46504612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76148888-C-T

http://identifiers.org/hco/21/GRCh38#46509156-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76143125-A-C

46509156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76143125-A-G

46509163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76143118-G-T

http://identifiers.org/hco/21/GRCh38#46509234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76143047-C-A

http://identifiers.org/hco/21/GRCh38#46509286-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76142995-A-C

46509286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76142995-A-G

46509364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76142917-G-A

46509364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 76142917-G-T

46509486-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76142807-G-C

46509507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76142789-T-C

46509508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76142788-G-T

http://identifiers.org/hco/21/GRCh38#46509771-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76142498-A-C

http://identifiers.org/hco/21/GRCh38#46511152-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76141262-A-C

46511152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76141262-A-G

46511154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76141260-G-A

46511261-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76141176-T-A

46511358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76141089-A-G

46511374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76141074-G-A

46511374-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76141074-G-C

46511374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76141074-G-T

http://identifiers.org/hco/21/GRCh38#46511499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76140963-C-A

46511499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76140963-C-T

46511584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76140878-A-G

46526786-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76139623-C-G

46526871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76139544-A-G

46527024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76139426-G-A

46527242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76139242-A-G

46527349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76139165-A-G

46527349-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76139165-A-T

46527350-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76139164-G-C

46527350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76139164-G-T

46527351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76139163-G-T

46527352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76139162-G-T

46527353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76139161-A-G

46527353-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76139161-A-T

46527543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76139093-C-T

46527610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76139036-G-A

46527778-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76138839-A-T

http://identifiers.org/hco/21/GRCh38#46527889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76138759-C-A

46528028-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76138619-T-G

46528276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76138555-T-C

46528333-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76138524-T-A

46528410-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76138439-T-G

46528903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76138309-G-A

46528959-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76138252-T-A

http://identifiers.org/hco/21/GRCh38#46529003-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76138214-A-C

46529003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76138214-A-G

46529016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76138204-T-C

46529016-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76138204-T-G

46529207-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76138012-G-C

46529207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76138012-G-T

46529208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76138011-T-C

46529253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76137966-A-G

46532259-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76135715-T-A

http://identifiers.org/hco/21/GRCh38#46532260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76135714-C-A

46532274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76135699-T-C

46532381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76135608-A-G

46532381-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76135608-A-T

46532438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76135572-G-T

46532492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76135547-G-A

46533135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76135002-A-G

http://identifiers.org/hco/21/GRCh38#46533147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76134991-C-A

46533421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76134726-T-C

http://identifiers.org/hco/21/GRCh38#46533479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76134682-C-A

46533502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76134659-A-G

46533502-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76134659-A-T

46533504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76134657-G-A

46533504-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76134657-G-C

46533616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76134533-G-A

46533744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76134405-T-C

46533786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76134365-T-C

http://identifiers.org/hco/21/GRCh38#46533881-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76134313-A-C

46533883-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76134311-T-A

46533906-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76134296-T-G

46533927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76134275-T-C

http://identifiers.org/hco/21/GRCh38#46533939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76134258-C-A

46533965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76134232-T-C

46533966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76134231-G-T

46534015-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76134183-C-G

46534338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76133872-G-A

46534339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76133871-A-G

http://identifiers.org/hco/21/GRCh38#46534531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76133742-C-A

46534531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76133742-C-T

http://identifiers.org/hco/21/GRCh38#46534716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76133560-C-A

http://identifiers.org/hco/21/GRCh38#46534748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76133529-C-A

http://identifiers.org/hco/21/GRCh38#46534772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76133519-C-A

46534772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76133519-C-T

46534956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76133344-G-A

46535069-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76133258-G-C

46535293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76133041-G-A

46535293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76133041-G-T

http://identifiers.org/hco/21/GRCh38#46537080-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76132391-A-C

46537080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76132391-A-G

46537178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76132295-A-G

46537363-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76132078-G-C

46537363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76132078-G-T

http://identifiers.org/hco/21/GRCh38#46537428-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76132013-A-C

46537428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76132013-A-G

46537488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76131950-C-T

46537553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76131881-T-C

46537617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76131820-A-G

46537631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76131806-G-T

46537663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76131771-G-A

46537663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76131771-G-T

http://identifiers.org/hco/21/GRCh38#46537682-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76131752-A-C

46537682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76131752-A-G

46537844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76131431-C-T

46538018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76131269-A-G

http://identifiers.org/hco/21/GRCh38#46538354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76130570-C-A

46538388-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76130539-A-T

46538431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76130497-A-G

46538497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76130431-G-A

46538497-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76130431-G-C

46538497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76130431-G-T

46538521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76130407-T-C

http://identifiers.org/hco/21/GRCh38#46538569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76130359-C-A

46538569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76130359-C-T

46538695-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76130200-T-G

http://identifiers.org/hco/21/GRCh38#46538870-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76130020-A-C

46538870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76130020-A-G

46538889-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76130001-T-A

46538889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76130001-T-C

http://identifiers.org/hco/21/GRCh38#46538922-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76129972-A-C

46538922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76129972-A-G

http://identifiers.org/hco/21/GRCh38#46538972-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76129922-A-C

46538972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76129922-A-G

46538972-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76129922-A-T

http://identifiers.org/hco/21/GRCh38#46538993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76129901-C-A

http://identifiers.org/hco/21/GRCh38#46539025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76129869-C-A

46539056-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76129841-T-A

46539056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76129841-T-C

http://identifiers.org/hco/21/GRCh38#46539068-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76129829-A-C

46539068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76129829-A-G

http://identifiers.org/hco/21/GRCh38#46539125-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76129784-A-C

46539196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76129713-C-T

http://identifiers.org/hco/21/GRCh38#46539205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76129704-C-A

46539205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76129704-C-T

46539221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76129688-A-G

46539221-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76129688-A-T

46539378-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76129627-T-G

46539413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76129590-A-G

46539430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76129573-G-A

46539825-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76128296-C-G

46539825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76128296-C-T

46540081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76128042-A-G

46540607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76127519-C-T

46541311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76127300-G-T

46541312-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76127299-A-T

46541433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76127214-C-T

46541671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76127059-G-A

http://identifiers.org/hco/21/GRCh38#46541700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76127033-C-A

46541713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76127022-C-T

http://identifiers.org/hco/21/GRCh38#46541720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76127015-C-A

46541720-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76127015-C-G

46541720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76127015-C-T

46541725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76127010-C-T

46541828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76126907-C-T

46541914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76126823-G-A

46545074-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76123344-A-T

46545355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76123070-G-A

46545355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76123070-G-T

46545372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76123053-G-A

46545372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76123053-G-T

46545382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76123042-C-T

46545413-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76122991-A-T

46545522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76122848-T-C

46545550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76122822-G-A

46545550-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76122822-G-C

46545777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76122450-A-G

46545953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76122202-A-G

46545984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76122165-G-A

46545985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 76122164-C-T

46546022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76122132-G-T

46546034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76122120-C-T

46546084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76122070-G-A

46546084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76122070-G-T

46546302-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76121913-T-A

http://identifiers.org/hco/21/GRCh38#46546337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76121880-C-A

46546337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76121880-C-T

46546416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76121830-G-A

46546416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76121830-G-T

46546458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76121797-G-A

46546571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76121687-C-T

46546697-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76121620-C-G

46546697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76121620-C-T

46546812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76121536-G-A

46546812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76121536-G-T

http://identifiers.org/hco/21/GRCh38#46546969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76121431-C-A

46546969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76121431-C-T

46547002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76121398-G-A

46547002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76121398-G-T

http://identifiers.org/hco/21/GRCh38#46547172-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76121260-A-C

46547200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76121229-A-G

46547291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76121139-G-A

46547291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76121139-G-T

http://identifiers.org/hco/21/GRCh38#46547293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76121137-C-A

http://identifiers.org/hco/21/GRCh38#46547296-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76121134-A-C

46547296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76121134-A-G

46547504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76120881-T-C

46548183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76120523-T-C

46548331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76120446-T-C

46548335-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76120442-T-G

46548601-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76120269-T-A

46548607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76120263-A-G

46549682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76118530-A-G

46549713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76118509-G-A

46549713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76118509-G-T

http://identifiers.org/hco/21/GRCh38#46549714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76118508-C-A

46549714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76118508-C-T

46549716-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76118506-T-G

46549746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76118485-G-A

46549746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76118485-G-T

46549799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76118431-C-T

46549830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76118400-A-G

46549832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76118398-C-T

46550335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76116900-G-A

http://identifiers.org/hco/21/GRCh38#46550478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76116772-C-A

46550478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76116772-C-T

http://identifiers.org/hco/21/GRCh38#46550493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76116758-C-A

46550493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76116758-C-T

46550591-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76116661-C-G

46550757-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76116498-T-A

46550770-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76116487-C-G

46550770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76116487-C-T

46550783-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76116474-C-G

http://identifiers.org/hco/21/GRCh38#46550886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76116374-C-A

46550886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76116374-C-T

46550909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76116362-C-T

46550910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76116361-G-A

46550955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76116331-C-G

46551558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76115878-A-G

46551574-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76115853-C-G

46551574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76115853-C-T

46551576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76115851-C-T

46551589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76115839-T-C

46551592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76115836-G-T

http://identifiers.org/hco/21/GRCh38#46551601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76115827-C-A

46551601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76115827-C-T

46551604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76115824-G-T

46551633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 76115799-G-A

46551687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76115745-G-A

46551687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76115745-G-T

46551818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 76115624-G-A

46551818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 76115624-G-T

46551839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76115603-G-A

46551924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76115522-A-G

http://identifiers.org/hco/21/GRCh38#46552036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76115509-C-A

46552036-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76115509-C-G

46552036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76115509-C-T

46552102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76115455-G-A

http://identifiers.org/hco/21/GRCh38#46552221-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76115337-A-C

46552221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76115337-A-G

46552441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76115074-G-A

46552474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76115051-A-G

46552537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76115004-G-A

46554193-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76114419-T-G

http://identifiers.org/hco/21/GRCh38#46554368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76114265-C-A

46554368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76114265-C-T

46554418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76114230-G-A

46554418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76114230-G-T

46554613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76112499-T-C

46554698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 76112414-T-C

46554704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 76112408-T-C

46554731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76112376-A-G

46554731-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76112376-A-T

http://identifiers.org/hco/21/GRCh38#46554753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76112354-C-A

46554753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76112354-C-T

46554781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76112322-G-A

46554781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76112322-G-T

46554834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76112260-G-A

46555005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76112076-G-A

46555005-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76112076-G-C

46555005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76112076-G-T

http://identifiers.org/hco/21/GRCh38#46555012-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76112069-A-C

46555012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76112069-A-G

46555113-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76111810-A-T

46555249-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76111643-C-G

46555395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76111541-G-T

46555440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76111499-G-A

46555440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76111499-G-T

46555447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76111485-G-T

46555454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76111478-A-G

http://identifiers.org/hco/21/GRCh38#46555467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76111467-C-A

46555467-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76111467-C-G

46555467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76111467-C-T

46555496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76111448-G-A

46555496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76111448-G-T

46555502-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76111441-T-A

46555508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76111435-C-T

46555556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76111325-G-A

46555556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76111325-G-T

46555570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76111308-G-A

46555570-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76111308-G-C

46555570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76111308-G-T

46555591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76111292-G-A

46555591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76111292-G-T

46555774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76111130-T-C

http://identifiers.org/hco/21/GRCh38#46555826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76111075-C-A

46555826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76111075-C-T

46555827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76111074-G-A

46555827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76111074-G-T

46556038-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76110874-C-G

46556105-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76110807-A-T

46556112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76110800-T-C

46556179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76110694-A-G

46556275-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76110600-T-G

http://identifiers.org/hco/21/GRCh38#46556756-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76110286-A-C

46556756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76110286-A-G

46556756-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76110286-A-T

46556758-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76110284-T-G

http://identifiers.org/hco/21/GRCh38#46556807-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76110236-A-C

46556807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76110236-A-G

46556807-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76110236-A-T

46556838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76110206-A-G

46556839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76110205-G-A

46556839-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76110205-G-C

46556839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76110205-G-T

http://identifiers.org/hco/21/GRCh38#46556840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76110204-C-A

46556840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76110204-C-T

46556841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76110203-T-C

46556848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76110195-T-C

http://identifiers.org/hco/21/GRCh38#46556851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76110192-C-A

46556851-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76110192-C-G

46556866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76110172-A-G

http://identifiers.org/hco/21/GRCh38#46556879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76110159-C-A

46556879-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76110159-C-G

46556879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76110159-C-T

http://identifiers.org/hco/21/GRCh38#46556888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76110150-C-A

46556888-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76110150-C-G

46556888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76110150-C-T

http://identifiers.org/hco/21/GRCh38#46556906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76110145-C-A

46556906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76110145-C-T

http://identifiers.org/hco/21/GRCh38#46556925-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76110126-A-C

46556925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76110126-A-G

46556925-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76110126-A-T

46556948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76110102-G-A

46556948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76110102-G-T

http://identifiers.org/hco/21/GRCh38#46556949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76110101-C-A

46556949-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76110101-C-G

46556949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76110101-C-T

http://identifiers.org/hco/21/GRCh38#46556952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76110098-C-A

46556952-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76110098-C-G

46556952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76110098-C-T

http://identifiers.org/hco/21/GRCh38#46557138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76109908-C-A

46557138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76109908-C-G

46557149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76109901-T-C

46557181-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76109870-T-A

46557303-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76109274-T-A

46557350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76109230-G-T

46557392-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76109189-T-G

46557430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76109151-G-A

46557430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76109151-G-T

46557460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76109133-T-C

46557460-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76109133-T-G

46557584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 76109036-G-A

46557584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 76109036-G-T

46557610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76109010-C-T

46557761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 76108859-C-T

http://identifiers.org/hco/21/GRCh38#46557798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76108841-C-A

46557798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76108841-C-T

46557918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76108826-G-A

46558066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76108716-C-T

46558145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76108612-G-T

46558201-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76108556-T-G

46558203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76108554-A-G

46558337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76108421-G-A

46558337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76108421-G-T

46558408-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76108350-G-C

46558478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76108273-G-T

46558493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76108261-A-G

46558493-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76108261-A-T

46558548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76108197-A-G

46558572-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76108173-T-A

46558572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76108173-T-C

http://identifiers.org/hco/21/GRCh38#46558657-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76108085-A-C

46558657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76108085-A-G

46558657-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76108085-A-T

46558828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76108011-G-T

46558859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76107981-G-A

http://identifiers.org/hco/21/GRCh38#46558863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76107977-C-A

46559042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76107953-A-G

46559080-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76107935-G-C

46559080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76107935-G-T

46559456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76107643-C-T

46560230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76106887-G-A

46560331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76106661-C-T

46560398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76106606-A-G

46560432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76106573-G-A

46560432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76106573-G-C

46560480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76106528-G-A

46560582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76106424-G-A

46560582-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76106424-G-C

46560582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76106424-G-T

46560641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76106368-G-A

46560641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76106368-G-T

http://identifiers.org/hco/21/GRCh38#46560734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76106277-C-A

46560734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76106277-C-T

46560793-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76106218-C-G

46560793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76106218-C-T

46562039-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76105783-C-G

46562095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76105727-G-T

46562184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76105643-C-T

http://identifiers.org/hco/21/GRCh38#46562467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76105447-C-A

46562467-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76105447-C-G

46563193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76104954-A-G

46563264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76104887-C-T

46563292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76104860-C-T

46563358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76104797-G-A

46563383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76104770-C-T

46563503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76104663-C-T

http://identifiers.org/hco/21/GRCh38#46563624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76104620-C-A

46563624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76104620-C-T

http://identifiers.org/hco/21/GRCh38#46563625-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76104619-A-C

46563625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76104619-A-G

46563625-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76104619-A-T

46563626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76104618-G-C

46563626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76104618-G-T

http://identifiers.org/hco/21/GRCh38#46563627-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76104617-A-C

46563627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76104617-A-G

46563704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76104532-G-T

46563719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76104517-G-A

46563719-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76104517-G-C

46563719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76104517-G-T

http://identifiers.org/hco/21/GRCh38#46563725-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76104511-A-C

46563725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76104511-A-G

46563725-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76104511-A-T

46563751-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76104486-T-A

46563751-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76104486-T-G

http://identifiers.org/hco/21/GRCh38#46563764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76104471-C-A

46563764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76104471-C-T

http://identifiers.org/hco/21/GRCh38#46563765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76104470-C-A

46563778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76104457-A-G

46563778-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76104457-A-T

http://identifiers.org/hco/21/GRCh38#46563793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76104438-C-A

46563945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76104312-C-T

46564008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76104232-A-G

46565553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76102465-A-G

46565557-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76102461-T-G

http://identifiers.org/hco/21/GRCh38#46565638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76102392-C-A

46565638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76102392-C-T

46565670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76102361-G-A

46565670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76102361-G-T

46565895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 76102141-G-A

46565955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76102048-G-A

46565975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76102028-A-G

46565975-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76102028-A-T

46566297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76101676-G-A

http://identifiers.org/hco/21/GRCh38#46566411-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76101564-A-C

46566411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76101564-A-G

46566489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76101522-C-T

http://identifiers.org/hco/21/GRCh38#46566727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76101289-C-A

46566728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76101288-C-T

http://identifiers.org/hco/21/GRCh38#46566769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76101253-C-A

46566769-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76101253-C-G

46566769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76101253-C-T

46566770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76101252-A-G

46566789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76101232-G-A

46566789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76101232-G-T

46566820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76101207-G-A

46566820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76101207-G-T

46566833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76101195-G-T

46567104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76100968-C-T

46567322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76100748-G-A

46567333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76100735-C-T

46567364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 76100711-C-T

46567625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 76100450-G-A

46567625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 76100450-G-T

http://identifiers.org/hco/21/GRCh38#46567630-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76100444-A-C

46567630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 76100444-A-G

46567630-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 76100444-A-T

http://identifiers.org/hco/21/GRCh38#46567649-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76100425-A-C

http://identifiers.org/hco/21/GRCh38#46567781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76100320-C-A

46567786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76100315-A-G

46567787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76100314-T-C

http://identifiers.org/hco/21/GRCh38#46567834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76100267-C-A

46567834-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76100267-C-G

46567834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76100267-C-T

46567873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76100237-G-A

46567873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76100237-G-T

46567883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76100227-G-A

46567883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76100227-G-T

http://identifiers.org/hco/21/GRCh38#46568055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76100065-C-A

46568612-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76099871-G-C

46568612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76099871-G-T

46568690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76099798-A-G

46569213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76099312-T-C

46569292-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76099266-A-T

46569295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76099263-T-C

46569322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76099239-C-T

46569739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76098850-T-C

http://identifiers.org/hco/21/GRCh38#46569753-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76098835-A-C

46569756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76098832-A-G

46569891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76098689-G-A

46569961-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76098626-T-A

46570002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76098584-G-C

46570234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17217
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76098361-G-A