39588427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117949035-G-T

39588450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117949056-G-A

39588460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117949069-A-G

http://identifiers.org/hco/15/GRCh38#39588560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#117949164-C-A

39588560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 117949164-C-T

39588644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 117949248-C-T

http://identifiers.org/hco/15/GRCh38#39588705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#117949309-C-A

39588705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117949309-C-T

39588783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117949403-G-T

39588935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117949538-A-G

39589077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 117949678-T-C

39589143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117949738-A-G

http://identifiers.org/hco/15/GRCh38#39589146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#117949747-C-A

39589146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117949747-C-T

http://identifiers.org/hco/15/GRCh38#39589193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#117949794-C-A

39589383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117949979-G-A

39589383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117949979-G-C

39589397-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117949993-T-G

http://identifiers.org/hco/15/GRCh38#39589789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#117950282-C-A

39589831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 117950324-G-A

39589840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 117950333-C-G

39589840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 117950333-C-T

39589888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 117950381-C-T

http://identifiers.org/hco/15/GRCh38#39590398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#117950614-C-A

39590398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117950614-C-T

39590443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117950645-G-A

39590462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117950662-A-G

39590473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117950673-A-G

http://identifiers.org/hco/15/GRCh38#39590542-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#117950729-A-C

39590542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 117950729-A-G

39590633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117950824-G-A

39590655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117950846-T-C

39590664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117950855-A-G

http://identifiers.org/hco/15/GRCh38#39590672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#117950863-C-A

39590991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117951138-A-G

39591012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117951154-T-C

39591012-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117951154-T-G

39591049-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117951173-A-T

39591057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117951181-T-C

39591058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117951182-G-A

39591058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117951182-G-T

39591143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117951270-T-C

39591444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117951547-C-T

http://identifiers.org/hco/15/GRCh38#39591745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#117951826-C-A

39591745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117951826-C-T

39591952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117951995-A-G

39591991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117952029-A-G

39592843-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117953190-C-G

39592928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117953281-G-A

39592930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117953283-G-A

39592949-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117953296-A-T

39592961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117953308-C-T

39593108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117953463-G-A

39593190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 117953545-C-T

http://identifiers.org/hco/15/GRCh38#39593236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#117953591-C-A

39593236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117953591-C-T

39593346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117953698-G-A

39593449-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 117953801-C-G

39593449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 117953801-C-T

39593479-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 117953831-C-G

39593611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 117953963-A-G

39593739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117954084-T-C

39593843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117954181-A-G

http://identifiers.org/hco/15/GRCh38#39593850-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#117954188-A-C

39593878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117954216-A-G

39593892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117954230-A-G

39594060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117954358-G-A

39594060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117954358-G-T

39594061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117954359-G-A

39594061-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117954359-G-C

39594061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117954359-G-T

http://identifiers.org/hco/15/GRCh38#39594076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#117954374-C-A

39594076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117954374-C-T

39594152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 117954450-C-G

39594179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 117954477-A-G

http://identifiers.org/hco/15/GRCh38#39594230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#117954527-C-A

39594511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117954801-T-C

39594651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117954933-T-C

39594825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117955095-G-A

39594825-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117955095-G-C

39595246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117955388-T-C

http://identifiers.org/hco/15/GRCh38#39595252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#117955394-C-A

39595252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117955394-C-T

39595281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117955422-G-A

39595281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117955422-G-T

39595312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117955459-T-C

39595313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117955460-A-G

39595409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117955536-G-A

39595409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117955536-G-T

39595427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117955554-G-A

39595427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117955554-G-T

39595461-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117955597-T-A

39595461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117955597-T-C

39595461-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117955597-T-G

39595545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117955679-A-G

39595545-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117955679-A-T

http://identifiers.org/hco/15/GRCh38#39595603-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#117955740-A-C

http://identifiers.org/hco/15/GRCh38#39595814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#117955961-C-A

39595814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 117955961-C-T

39595939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 117956074-A-G

39596048-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 117956177-T-G

39596066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 117956195-G-A

39596066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 117956195-G-T

http://identifiers.org/hco/15/GRCh38#39596080-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#117956207-A-C

39596102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 117956220-G-A

39596102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 117956220-G-T

39596822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 117956959-A-G

39596924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 117957056-G-T

39597247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 117957377-G-T

39597325-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 117957463-A-T

39597351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 117957491-G-A

39597596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 117957730-T-C

39597719-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 117957830-T-A

http://identifiers.org/hco/15/GRCh38#39597728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#117957839-C-A

39597777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 117957897-T-C

http://identifiers.org/hco/15/GRCh38#39597871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#117958039-C-A

39597871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 117958039-C-T

39597936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 117958144-A-G

39598146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 117958441-G-T

39598337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 117958598-A-G

http://identifiers.org/hco/15/GRCh38#39598338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#117958599-C-A

39598354-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 117958616-A-T

http://identifiers.org/hco/15/GRCh38#39598575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#117958806-C-A

39598597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 117958854-G-A

39598749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 117959003-G-A

39598749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 117959003-G-T

39598821-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 117959069-A-T

39598880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 117959116-T-C

http://identifiers.org/hco/15/GRCh38#39598900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#117959153-C-A

39598911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 117959164-T-C

http://identifiers.org/hco/15/GRCh38#39598928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#117959175-C-A

39598928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 117959175-C-T

39598930-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 117959177-T-A

39598932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 117959179-T-C

http://identifiers.org/hco/15/GRCh38#39598934-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#117959181-A-C

39598934-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 117959181-A-T

39598983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 117959194-A-G

39598983-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 117959194-A-T

39598987-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 117959198-T-A

39599048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 117959232-C-T

http://identifiers.org/hco/15/GRCh38#39599421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#117959495-C-A

39599452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 117959520-T-C

39599474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 117959545-G-A

39599474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 117959545-G-T

39599553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 117959598-C-T

39599775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 117959818-A-G

39600137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 117960238-G-T

39600373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 117960454-A-G

http://identifiers.org/hco/15/GRCh38#39600781-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#117960949-A-C

39600781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 117960949-A-G

39600800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 117960968-T-C

39600811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 117960979-T-C

39600831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 117960998-T-C

39600893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 117961060-C-T

http://identifiers.org/hco/15/GRCh38#39600894-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#117961061-A-C

39600894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 117961061-A-G

39600915-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 117961082-T-A

http://identifiers.org/hco/15/GRCh38#39601069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#117961235-C-A

http://identifiers.org/hco/15/GRCh38#39601078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#117961239-C-A

39601118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117961266-G-A

39601118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117961266-G-T

39601400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117961546-A-G

39601459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117961596-T-C

39601465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117961602-G-A

39601513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117961631-G-A

39601541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117961650-C-T

http://identifiers.org/hco/15/GRCh38#39601700-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#117961802-A-C

39601802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117961909-T-C

39601805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117961912-G-A

39601830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117961937-T-C

39601838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117961945-C-T

39601860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117961967-A-G

39602622-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117962031-T-G

39602697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117962118-G-A

39602697-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117962118-G-C

39602803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117962242-T-C

39602902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117962308-C-T

39602950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117962341-T-C

39602973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117962376-C-T

39603193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117962583-T-C

http://identifiers.org/hco/15/GRCh38#39616918-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#117965663-A-C

39616951-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117965707-C-G

http://identifiers.org/hco/15/GRCh38#39616952-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#117965708-A-C

http://identifiers.org/hco/15/GRCh38#39617078-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#117965984-A-C

39617078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117965984-A-G

39617246-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117966148-T-G

39617347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117966246-C-T

39617349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117966248-A-G

39617359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117966267-T-C

39617451-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117966333-T-G

39617496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117966378-T-C

39617611-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117966477-T-G

http://identifiers.org/hco/15/GRCh38#39617672-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#117966536-A-C

39617687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117966551-G-A

39617687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117966551-G-T

39617741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 117966601-T-C

39617741-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 117966601-T-G

39617801-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 117966661-T-A

39617878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 117966738-T-C

39617882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 117966742-T-C

39617939-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 117966799-T-A

39618078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 117966938-C-T

39618086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 117966946-A-G

39618193-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 117967053-T-G

39618310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117967170-G-A

39618310-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117967170-G-C

39618310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117967170-G-T

http://identifiers.org/hco/15/GRCh38#39618390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#117967255-C-A

39618489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117967656-T-C

39618637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117967824-G-A

39618696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117967877-G-A

39619609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117969588-T-C

39620102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117970053-C-T

39621945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117970645-T-C

39622935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117976984-G-A

39623128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117977193-C-T

39623171-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117977233-C-G

39623360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117977416-G-T

39623568-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117977641-T-A

39623568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117977641-T-C

39623603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117977673-A-G

39626994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117978128-C-T

http://identifiers.org/hco/15/GRCh38#39627145-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#117978259-A-C

39627168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117978274-G-A

39627723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117978434-G-A

39627723-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117978434-G-C

39627917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117978576-G-T

39628001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117978621-T-C

39628029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117978638-T-C

http://identifiers.org/hco/15/GRCh38#39628121-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#117978722-A-C

39628234-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, undefined
orthologous variants: 117978830-C-G

39628535-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117979091-T-G

39628553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117979109-T-C

39628588-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117979144-T-G

39628593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117979153-G-A

39628615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117979176-G-A

39628773-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117979584-G-C

39628806-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117979618-C-G

39628938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117979748-A-G

39628967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117979777-A-G

39629736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117980457-C-T

39629794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117980514-A-G

39630265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117980964-T-C

http://identifiers.org/hco/15/GRCh38#39630543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#117981215-C-A

http://identifiers.org/hco/15/GRCh38#39630555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#117981227-C-A

http://identifiers.org/hco/15/GRCh38#39630839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#117981398-C-A

39630839-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117981398-C-G

39630839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117981398-C-T

39630990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117981517-G-C

39631023-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117981550-G-C

39631198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117981897-C-T

39631256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117981950-C-T

39631340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117982019-T-C

39631508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117982173-T-C

39631554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117982246-G-A

http://identifiers.org/hco/15/GRCh38#39631581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#117982282-C-A

39631854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117982552-C-T

39631964-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117982657-G-C

http://identifiers.org/hco/15/GRCh38#39631983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#117982675-C-A

39631983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117982675-C-T

39632084-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117982768-G-C

39635829-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117984408-C-G

39635890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117984451-T-C

39635969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117984524-T-C

39636070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117984630-A-G

39636352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117984897-T-C

39636729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117985249-C-T

39636834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117985314-T-C

39636849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117985328-G-A

39637026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117985490-G-A

39637266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117985722-C-T

39638087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117987010-T-C

39638270-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117987196-T-G

39638316-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117987239-C-G

39638354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117987277-C-T

39638842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117988540-A-G

39638934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117988616-C-T

39638953-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117988676-C-G

39638953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117988676-C-T

39639125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117988814-T-C

http://identifiers.org/hco/15/GRCh38#39639156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#117988845-C-A

39639156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117988845-C-T

39639211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117988899-T-C

39639445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117989096-G-A

39641588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117990305-G-A

39641670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117990395-T-C

39641671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117990396-G-A

http://identifiers.org/hco/15/GRCh38#39641678-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#117990403-A-C

http://identifiers.org/hco/15/GRCh38#39641845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#117990734-C-A

39641984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117990872-G-A

39641994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117990882-G-A

39641998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117990886-C-T

39642099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117990986-G-A

39642099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117990986-G-T

39642166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117991044-A-G

39642216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117991065-G-A

39642618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117991432-C-T

39642853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117991885-T-C

39643597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117992485-T-C

39643765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117992618-T-C

39644252-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117993098-C-G

39644340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117993186-T-C

39644523-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117993373-C-G

39644524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117993374-G-A

39644524-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117993374-G-C

39644553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117993403-A-G

39644652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117993488-G-A

39644673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117993509-T-C

39644976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117993819-G-A

39647714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117994062-C-T

39647843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117994171-T-C

http://identifiers.org/hco/15/GRCh38#39648032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#117994287-C-A

39648032-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117994287-C-G

39648032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117994287-C-T

http://identifiers.org/hco/15/GRCh38#39648336-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#117994520-A-C

39648928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117994736-G-A

39649063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117994836-A-G

39649135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117994910-G-A

39649135-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117994910-G-C

39649370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117995116-T-C

39649373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117995119-C-T

39649559-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117995277-A-T

39649560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117995278-T-C

39649572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117995291-C-T

http://identifiers.org/hco/15/GRCh38#39649641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#117995357-C-A

39649671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117995385-A-G

39649878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117995588-C-T

39649894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117995604-G-A

39649929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117995639-C-T

39649937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117995646-C-T

39650023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117995742-C-T

39650043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117995762-G-A

39650574-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117997584-T-G

39650629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117997639-C-T

39650850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117999747-C-T

39650852-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117999749-T-G

39650919-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 117999812-G-C

39652586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118000505-T-C

39652590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118000509-C-T

39658783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118002511-C-T

http://identifiers.org/hco/15/GRCh38#39658806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118002531-C-A

39661157-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118004768-G-C

39661488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118005032-T-C

39661504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118005050-A-G

39661593-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118005157-T-A

39661608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118005172-A-G

39661697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118005260-C-T

39661772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118005313-T-C

39661793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118005334-T-C

39661877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118005416-G-A

39661981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118005521-T-C

39662129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118005646-A-G

39662264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118005780-G-A

39662418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118005953-A-G

39662422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118005957-T-C

39662462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118005997-T-C

39662512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118006025-C-T

39662548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118006608-A-G

39662595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118006654-T-C

39662645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118006686-C-T

39663939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118006970-A-G

39664010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118007037-G-A

39664070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118007100-G-A

39664072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118007102-G-A

39664153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118007179-C-T

39664192-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118007217-A-T

39664327-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118007349-G-C

39664394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118007417-T-C

39664486-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118007507-T-A

39664958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118007852-A-G

39665073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118007916-T-C

39665088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118007928-A-G

http://identifiers.org/hco/15/GRCh38#39665244-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118008129-A-C

http://identifiers.org/hco/15/GRCh38#39665319-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118008191-A-C

39666260-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118009572-T-A

39666429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118009729-G-A

39666755-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, undefined
orthologous variants: 118010005-T-A

39666756-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, undefined
orthologous variants: 118010006-C-G

39666816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, undefined
orthologous variants: 118010110-C-T

39666868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, undefined
orthologous variants: 118010165-G-A

39670233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118012391-G-A

39670396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118012529-A-G

39670445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118012578-A-G

39670850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118012976-C-T

39671531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118013612-A-G

39671558-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118013639-T-G

39671644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118013726-A-G

39671812-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118013890-T-A

39671812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118013890-T-C

39671959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118014036-C-T

39671962-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118014039-G-C

39671962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118014039-G-T

http://identifiers.org/hco/15/GRCh38#39672015-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118014093-A-C

39672015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118014093-A-G

39672046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118014122-G-T

39672240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118014298-A-G

39672240-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118014298-A-T

39673198-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118018426-T-A

39673257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118018485-T-C

39675716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118021691-T-C

http://identifiers.org/hco/15/GRCh38#39676927-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118023287-A-C

39677174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118023499-G-A

39677730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118024107-G-A

39677857-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118024304-G-C

39677865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118024312-G-A

39677868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118024315-T-C

39677897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118024354-G-A

39677899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118024356-G-A

39677982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118024425-G-A

http://identifiers.org/hco/15/GRCh38#39678396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118024840-C-A

39678412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118024855-A-G

39678618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118025044-G-A

39678633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118025059-T-C

39679662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118026042-A-G

39679673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118026051-C-T

39679685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118026063-A-G

39679772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118026148-A-G

39679794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118026170-G-A

39679794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118026170-G-T

39679814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118026190-A-G

39679903-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118026256-T-G

http://identifiers.org/hco/15/GRCh38#39679950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118026304-C-A

39679950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118026304-C-T

39679997-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118026350-G-C

39680114-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118026451-A-T

39680227-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118026562-A-T

39680385-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118026704-C-G

39680519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118026809-G-A

39682118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118028991-G-A

39682136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118029009-C-T

39682201-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118029059-T-A

39682342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118029201-C-T

http://identifiers.org/hco/15/GRCh38#39685429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118029824-C-A

39685429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118029824-C-T

39685440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118029827-A-G

39685457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118029836-G-A

39685612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118030001-A-G

39685946-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118030251-T-G

http://identifiers.org/hco/15/GRCh38#39686163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118030496-C-A

39686201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118030539-A-G

39686232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118030560-T-C

39686373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118030702-A-G

39686573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118031860-G-T

http://identifiers.org/hco/15/GRCh38#39686602-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118031918-A-C

http://identifiers.org/hco/15/GRCh38#39686603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118031919-C-A

39687118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118032360-C-T

39691356-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118032593-G-C

39691509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118032774-G-A

39691607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118032883-G-T

39691739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118033012-T-C

39691762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118033040-G-A

39691827-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118033101-C-G

39691897-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118033231-G-C

39691909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118033243-T-C

39692069-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118033435-T-A

39692297-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118033728-T-A

39692431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118033865-T-C

39693225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, undefined
orthologous variants: 118034620-C-T

39693374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118034767-T-C

39693388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, undefined
orthologous variants: 118034781-G-A

39693429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118034822-T-C

39693645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118035049-C-T

39693668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118035074-T-C

39693914-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118035312-G-C

39693939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118035337-T-C

39694187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 118035569-C-T

39694279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 118035644-G-A

39695136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 118036004-T-C

39695173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 118036031-A-G

39695314-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 118036122-C-G

39695346-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 118036153-T-G

39695394-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 118036198-G-C

39695453-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 118036250-T-G

39695676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 118036674-A-G

39695732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 118036727-A-G

39695747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 118036739-G-T

39695798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 118036790-G-A

39696143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 118037132-A-G

39696363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 118037308-C-T

39696420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 118037363-T-C

39696654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 118038183-T-C

http://identifiers.org/hco/15/GRCh38#39696794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118038557-C-A

39696851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 118038614-G-A

39696851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 118038614-G-T

39696856-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 118038619-G-C

39696876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 118038662-G-C

39696896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 118038682-G-A

39696912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 118038698-G-A

39696912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 118038698-G-T

39696914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 118038700-G-T

39696920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 118038706-G-A

39696942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 118038730-G-T

39696944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 118038732-A-G

39697211-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 118038989-A-T

39697282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 118039161-G-T

39697331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 118039201-T-C

39697374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 118039244-T-C

http://identifiers.org/hco/15/GRCh38#39697484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118039343-C-A

39697564-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, missense_variant
orthologous variants: 118039416-G-C

39697882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118039751-C-T

39698178-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118039871-T-A

39698326-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118039970-T-G

39698360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118039999-G-A

39698374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118040013-T-C

http://identifiers.org/hco/15/GRCh38#39698470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118040099-C-A

39698838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118040411-A-G

39699038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, undefined
orthologous variants: 118040587-C-T

39699156-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118040702-G-C

39699217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118040774-T-C

39699257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, undefined
orthologous variants: 118040810-A-G

39699355-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118040897-T-A

39699670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118041202-C-T

39699820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118041338-C-T

http://identifiers.org/hco/15/GRCh38#39699833-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118041351-A-C

39699876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118041394-A-G

39699896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118041415-G-A

39699900-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118041419-T-G

39700025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118041507-C-T

39700082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118041563-A-G

39700307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118041769-A-G

39701563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118043906-G-A

39701950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118044276-G-A

39702007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118044311-A-G

39702151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118044439-T-C

39702296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118044583-A-G

http://identifiers.org/hco/15/GRCh38#39702382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118044648-C-A

39704596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118048609-G-A

39704612-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118048625-G-C

39704650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, undefined
orthologous variants: 118048664-A-G

39704673-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, undefined
orthologous variants: 118048674-G-C

39704745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118048735-C-T

39704844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118048834-A-G

39704965-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118048947-A-T

39705288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118049265-A-G

http://identifiers.org/hco/15/GRCh38#39705333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118049295-C-A

39706363-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118049769-C-G

39706475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118049858-G-T

39706650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118050008-A-G

http://identifiers.org/hco/15/GRCh38#39706892-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118050207-A-C

39707043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118050370-G-A

39707443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118050984-C-T

39707461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118051002-G-A

39707843-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118051815-A-T

39707975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118051959-G-A

http://identifiers.org/hco/15/GRCh38#39709266-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118052097-A-C

39712848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118052412-T-C

39713124-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118052622-T-A

http://identifiers.org/hco/15/GRCh38#39713443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: splice donor variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118052803-C-A

39713443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: splice donor variant
orthologous variants: 118052803-C-T

39713540-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: synonymous variant
orthologous variants: 118052900-T-A

39713540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: synonymous variant
orthologous variants: 118052900-T-C

39713540-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: synonymous variant
orthologous variants: 118052900-T-G

39713578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: missense variant
orthologous variants: 118052938-G-A

39713578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: missense variant
orthologous variants: 118052938-G-T

39713587-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 118052947-T-A

39713607-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118052989-T-A

39713607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118052989-T-C

39713607-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118052989-T-G

39713617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118053007-G-A

39713617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118053007-G-T

39713743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118053130-G-A

39718856-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118054347-T-A

39718875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118054366-C-T

39719008-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118054476-A-T

39719014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118054482-A-G

http://identifiers.org/hco/15/GRCh38#39719060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118054528-C-A

39719074-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118054542-T-G

39719122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118054588-G-A

39719131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118054603-G-T

39719579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118055027-A-G

39719786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118055194-G-T

39719911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118055313-G-A

39719911-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118055313-G-C

http://identifiers.org/hco/15/GRCh38#39720076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118055504-C-A

39720293-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118055668-G-C

http://identifiers.org/hco/15/GRCh38#39720308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118055682-C-A

39720308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118055682-C-T

39720621-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118056006-G-C

39720827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118056206-G-A

39720853-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118056234-T-A

http://identifiers.org/hco/15/GRCh38#39720899-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#118056280-A-C

39720899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, undefined
orthologous variants: 118056280-A-G

39721161-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, undefined
orthologous variants: 118056537-C-G

39721171-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, undefined
orthologous variants: 118056546-T-G

39721244-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, undefined
orthologous variants: 118056586-C-G

39721246-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, undefined
orthologous variants: 118056588-T-A

39721246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, undefined
orthologous variants: 118056588-T-C

http://identifiers.org/hco/15/GRCh38#39721270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#118056612-C-A

39721279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, undefined
orthologous variants: 118056620-G-A

39721295-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118056636-T-A

http://identifiers.org/hco/15/GRCh38#39723610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118059015-C-A

39723689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118059296-G-A

39723757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118059366-T-C

39724053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118059663-A-G

39724062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118059671-C-T

39724127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118060297-G-A

39724911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118060680-T-C

39724960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118060729-C-T

39726389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118061513-A-G

39726407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118061531-C-T

39726451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118061575-G-T

http://identifiers.org/hco/15/GRCh38#39726458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118061582-C-A

39726542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118061672-A-G

39726543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118061673-G-T

39726544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118061674-C-T

39726630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: missense variant
orthologous variants: 118063423-T-C

http://identifiers.org/hco/15/GRCh38#39726719-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118063512-A-C

39726831-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118063626-A-T

http://identifiers.org/hco/15/GRCh38#39726852-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118063636-A-C

39726852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118063636-A-G

39726852-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118063636-A-T

39726952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118063701-G-A

39726952-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118063701-G-C

39727035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118063755-T-C

39727112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118063806-T-C

39731557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118064865-T-C

39731561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118064869-T-C

39731702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118065009-T-C

39734991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118066193-A-G

39735036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118066241-C-T

39737027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118066818-G-A

39737027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118066818-G-T

39737036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118066827-A-G

39737043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118066834-C-T

39737232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118067023-C-T

39737252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118067043-G-A

39737252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118067043-G-T

39737451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118067164-C-T

http://identifiers.org/hco/15/GRCh38#39738086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118067390-C-A

39738086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118067390-C-T

39738103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: synonymous variant
orthologous variants: 118067407-G-A

39738103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: synonymous variant
orthologous variants: 118067407-G-T

39738136-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: synonymous variant
orthologous variants: 118067440-A-T

http://identifiers.org/hco/15/GRCh38#39738205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118067509-C-A

39738205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 118067509-C-T

http://identifiers.org/hco/15/GRCh38#39738233-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118067536-A-C

39738233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118067536-A-G

39738233-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118067536-A-T

39738247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118067550-A-G

39738255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118067558-G-A

39738255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118067558-G-T

39738256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118067559-G-A

39738256-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118067559-G-C

39738256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118067559-G-T

http://identifiers.org/hco/15/GRCh38#39738961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118068834-C-A

39739015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118068892-T-C

39739027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118068905-C-T

39739130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118069011-T-C

http://identifiers.org/hco/15/GRCh38#39739139-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118069022-A-C

39739325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118069222-A-G

39739349-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118069246-G-C

39739402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118069282-C-T

39739662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118070870-T-C

39739795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 118071036-A-G

39739828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118071069-A-G

http://identifiers.org/hco/15/GRCh38#39739841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118071082-C-A

39739841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118071082-C-T

39739922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118071160-C-T

39741721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118072040-G-A

39741721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118072040-G-T

http://identifiers.org/hco/15/GRCh38#39741756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118072076-C-A

39741777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118072097-G-A

39741777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118072097-G-T

39741913-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118072238-A-T

39741966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118072281-G-T

39741987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118072309-A-G

39741987-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118072309-A-T

39753504-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118075401-T-A

39753575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118075471-A-G

39753582-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118075478-T-A

39753582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118075478-T-C

39753583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118075479-C-T

39753856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118075753-C-T

39754197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118076115-A-G

39754252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118076170-A-G

39754282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118076200-C-T

39754492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118076375-T-C

39763368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118078379-G-A

39763417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118078427-G-A

http://identifiers.org/hco/15/GRCh38#39763430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118078440-C-A

39763593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118078591-C-T

39763660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118078653-T-C

39763683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118078676-T-C

39763686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118078679-G-T

39763730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118078723-G-A

39763730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118078723-G-T

39763802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118078757-G-A

39763802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118078757-G-T

39763825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: synonymous variant
orthologous variants: 118078780-A-G

39763825-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: synonymous variant
orthologous variants: 118078780-A-T

39763918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 118078876-A-G

39763936-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118078894-T-G

39763970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118078928-T-C

http://identifiers.org/hco/15/GRCh38#39763990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118078945-C-A

39763990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118078945-C-T

http://identifiers.org/hco/15/GRCh38#39763995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118078950-C-A

39763995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118078950-C-T

39764045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118079004-G-A

39764045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118079004-G-T

39764046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118079005-G-A

39764046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118079005-G-T

39764048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118079007-A-G

39764048-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118079007-A-T

39764053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118079012-G-A

39764053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118079012-G-T

39764242-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118079340-T-A

http://identifiers.org/hco/15/GRCh38#39764300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118079399-C-A

39764300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118079399-C-T

39764366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118079448-C-T

39764456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118079528-C-T

39764508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118079579-G-A

39764515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118079586-G-A

39764515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118079586-G-T

39764637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118079699-T-C

39764761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118079820-C-T

39764918-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118079972-T-A

39764946-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118080000-C-G

39765095-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118080130-G-C

39765095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118080130-G-T

39765116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118080151-A-G

39765151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118080183-G-T

http://identifiers.org/hco/15/GRCh38#39765634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118080329-C-A

39765634-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: missense variant
orthologous variants: 118080329-C-G

39765634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: synonymous variant
orthologous variants: 118080329-C-T

39765788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118080487-A-G

39765788-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118080487-A-T

http://identifiers.org/hco/15/GRCh38#39765791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118080490-C-A

39765869-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118080564-T-A

39765869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118080564-T-C

39766027-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118080671-A-T

http://identifiers.org/hco/15/GRCh38#39766047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118080691-C-A

39766193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118080830-C-T

http://identifiers.org/hco/15/GRCh38#39766223-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118080858-A-C

39766426-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118081115-T-G

39766548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118081205-G-A

39767172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118081469-A-G

39767354-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118081603-T-G

39769843-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118081755-T-G

http://identifiers.org/hco/15/GRCh38#39770286-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118082059-A-C

39770286-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118082059-A-T

39770360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118082073-T-C

39770380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118082077-T-C

http://identifiers.org/hco/15/GRCh38#39770614-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118082304-A-C

39770614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 118082304-A-G

39770648-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118082469-T-A

39770648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118082469-T-C

39770648-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118082469-T-G

http://identifiers.org/hco/15/GRCh38#39770649-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118082470-A-C

39770649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118082470-A-G

39770649-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118082470-A-T

39770660-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118082521-T-A

39770660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118082521-T-C

39770661-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118082522-T-A

http://identifiers.org/hco/15/GRCh38#39770662-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118082523-A-C

39770662-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118082523-A-T

http://identifiers.org/hco/15/GRCh38#39770724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118082582-C-A

39770724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118082582-C-T

http://identifiers.org/hco/15/GRCh38#39770754-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118082611-A-C

39770816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118082683-T-C

39770905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118082735-C-T

http://identifiers.org/hco/15/GRCh38#39770957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118082759-C-A

39771048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118082855-G-A

39771430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118083163-A-G

http://identifiers.org/hco/15/GRCh38#39771431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118083164-C-A

39771443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118083179-G-T

39771451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118083187-G-A

39775971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118083533-G-A

39775971-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118083533-G-C

39776407-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: missense variant
orthologous variants: 118083775-A-T

39776441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: synonymous variant
orthologous variants: 118083809-A-G

39776498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: synonymous variant
orthologous variants: 118083866-A-G

39776498-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: missense variant
orthologous variants: 118083866-A-T

http://identifiers.org/hco/15/GRCh38#39776656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118084007-C-A

39777299-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118084338-G-C

39778059-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118085037-T-A

39778308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118085287-A-G

39778489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118085458-G-A

39778714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118085673-T-C

39778728-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118085686-C-G

39778728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: 118085686-C-T

39782205-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118086895-G-C

39782237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118086932-G-A

39782365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118087037-G-A

39782384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118087052-G-A

39782384-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118087052-G-C

39782440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118087095-G-A

39782446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118087101-G-A

39782446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118087101-G-T

39782448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118087103-G-A

39782448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118087103-G-T

39782449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118087104-G-A

39782449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118087104-G-T

39782450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118087105-A-G

http://identifiers.org/hco/15/GRCh38#39782501-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118087195-A-C

http://identifiers.org/hco/15/GRCh38#39782620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#118087302-C-A

39782620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 118087302-C-T