241188514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: 5 prime UTR variant
orthologous variants: 93301523-T-C

http://identifiers.org/hco/2/GRCh38#241188588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93301603-C-A

241188588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: 5 prime UTR variant
orthologous variants: 93301603-C-T

241188648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 93301668-G-A

241188648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 93301668-G-T

241188680-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 93301676-G-C

241188698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 93301701-C-T

241188791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93301800-G-A

241188852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93301844-G-A

241188852-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93301844-G-C

241188852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93301844-G-T

241188885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93301873-A-G

241189201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93302152-G-A

241189362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93302251-C-T

241189800-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93302577-T-G

241189856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93302635-G-A

241189997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93302789-G-A

http://identifiers.org/hco/2/GRCh38#241190080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93302880-C-A

241190080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93302880-C-T

http://identifiers.org/hco/2/GRCh38#241190096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93302896-C-A

241190096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93302896-C-G

241190096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 93302896-C-T

http://identifiers.org/hco/2/GRCh38#241190183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93302985-C-A

241190572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93304271-T-C

241190704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93304363-G-A

241190704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93304363-G-T

241191032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93304704-C-T

241191085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93304756-G-A

241191085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93304756-G-T

241191120-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93304882-T-G

241191141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93304944-G-A

241191141-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93304944-G-C

241191141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93304944-G-T

241191381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93305185-A-G

241191381-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93305185-A-T

http://identifiers.org/hco/2/GRCh38#241191389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93305191-C-A

241191389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93305191-C-T

http://identifiers.org/hco/2/GRCh38#241191502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93305292-C-A

241191560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93305357-C-T

241191607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93305403-A-G

241191660-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93305458-C-G

241191660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93305458-C-T

241195404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93307790-T-C

241195404-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93307790-T-G

241195566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93307923-G-A

241195566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93307923-G-T

241195598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93307947-G-T

241195635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93308061-G-A

241195635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93308061-G-T

241195874-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 93308293-C-G

http://identifiers.org/hco/2/GRCh38#241195876-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93308295-A-C

241195941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93308357-G-A

241195941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93308357-G-T

241195966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93308382-G-A

241195975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93308391-G-T

http://identifiers.org/hco/2/GRCh38#241195989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93308405-C-A

241195989-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93308405-C-G

241195989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93308405-C-T

241196011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93308424-G-T

241196096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93308511-C-T

241196113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93308527-T-C

241196174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93308581-G-A

241196174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93308581-G-T

http://identifiers.org/hco/2/GRCh38#241196217-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93308620-A-C

241196304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93308693-G-A

241196304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93308693-G-T

241196314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93308703-G-A

241196314-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93308703-G-C

241196314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93308703-G-T

241196426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93308803-G-A

241196426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93308803-G-T

http://identifiers.org/hco/2/GRCh38#241198975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93312192-C-A

241198975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93312192-C-T

241199045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93312300-G-A

241199047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93312302-G-A

http://identifiers.org/hco/2/GRCh38#241199078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93312333-C-A

241199078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93312333-C-T

241199135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93312359-G-A

241199135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93312359-G-T

241199192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93312411-A-G

241199192-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93312411-A-T

241199199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93312421-G-T

http://identifiers.org/hco/2/GRCh38#241199200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93312422-C-A

241199200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93312422-C-T

241199231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93312460-T-C

241199295-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93312511-C-G

241199295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93312511-C-T

241199363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 93312580-C-T

241199435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93312652-G-A

241199439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93312656-G-A

241199465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93312682-G-A

241199465-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93312682-G-C

http://identifiers.org/hco/2/GRCh38#241199572-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93312807-A-C

http://identifiers.org/hco/2/GRCh38#241199574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93312809-C-A

241199574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93312809-C-T

http://identifiers.org/hco/2/GRCh38#241199660-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93312902-A-C

241199720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93312967-C-T

http://identifiers.org/hco/2/GRCh38#241199740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93312988-C-A

http://identifiers.org/hco/2/GRCh38#241199754-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93313002-A-C

241199779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93313020-C-T

http://identifiers.org/hco/2/GRCh38#241199815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93313051-C-A

241199816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93313052-G-A

241199921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93313156-A-G

241199997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93313198-G-A

241199997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93313198-G-T

241200106-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 93313286-C-G

241200121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 93313301-C-T

241200287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93313503-G-T

http://identifiers.org/hco/2/GRCh38#241200304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93313520-C-A

241200304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93313520-C-T

http://identifiers.org/hco/2/GRCh38#241200320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93313539-C-A

241200337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93313556-G-A

241200337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93313556-G-T

241200364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93313581-G-A

241200364-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93313581-G-C

241200392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93313609-C-T

241200393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93313610-C-T

241200425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93313643-G-T

241201369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93315028-C-T

http://identifiers.org/hco/2/GRCh38#241201444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93315105-C-A

241201444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93315105-C-T

241201488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93315135-G-A

241201488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93315135-G-C

241201488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93315135-G-T

241201515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93315163-G-A

241202115-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93316260-T-A

241202115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93316260-T-C

241202190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 93316315-G-A

241202298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 93316423-G-A

241202298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 93316423-G-T

241202387-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93316508-T-A

241202387-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93316508-T-G

http://identifiers.org/hco/2/GRCh38#241202417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93316538-C-A

241202417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93316538-C-T

http://identifiers.org/hco/2/GRCh38#241202437-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93316559-A-C

241202438-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93316560-T-A

241202438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93316560-T-C

241202605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93316683-G-A

241202605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93316683-G-T

http://identifiers.org/hco/2/GRCh38#241202753-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93316824-A-C

241202789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93316860-C-T

241203031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93317679-G-A

241203083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93317734-G-A

241203109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93317762-G-A

241203379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93318047-A-G

http://identifiers.org/hco/2/GRCh38#241203646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93318232-C-A

241203646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93318232-C-T

241203648-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93318234-T-A

241203785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93318330-G-T

241203840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93318391-T-C

241203897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93318440-A-G

http://identifiers.org/hco/2/GRCh38#241203899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93318442-C-A

241203899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93318442-C-T

241204200-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93318524-A-T

241204320-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93318648-C-G

http://identifiers.org/hco/2/GRCh38#241204341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93318669-C-A

241204360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93318683-G-A

241204360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93318683-G-T

http://identifiers.org/hco/2/GRCh38#241204421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93318749-C-A

241204421-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93318749-C-G

241204434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93318755-G-A

241204564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93318862-G-A

241204657-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93318955-T-A

241204657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93318955-T-C

241204688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93318986-G-A

241204718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93319009-T-C

http://identifiers.org/hco/2/GRCh38#241204844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93319104-C-A

241204844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93319104-C-T

241204893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 93319151-G-A

241205068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93319309-A-G

241205076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93319317-G-A

241205076-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93319317-G-C

241205130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93319358-G-A

241205211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93319436-G-A

241207555-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93319907-T-A

241207684-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 93320033-T-G

241207746-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93320078-G-C

241207746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93320078-G-T

241209226-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 93321997-G-C

241209226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 93321997-G-T

241209261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained, synonymous_variant
orthologous variants: 93322038-G-A

241209261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93322038-G-T

http://identifiers.org/hco/2/GRCh38#241209308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93322082-C-A

241209308-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 93322082-C-G

241209308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 93322082-C-T

http://identifiers.org/hco/2/GRCh38#241209314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93322088-C-A

241209314-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 93322088-C-G

241209314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 93322088-C-T

241209371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 93322145-G-A

241209371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93322145-G-T

241209373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 93322147-G-A

241209373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: missense_variant, non_coding_transcript_exon_variant, stop_gained, synonymous_variant
orthologous variants: 93322147-G-T

http://identifiers.org/hco/2/GRCh38#241209380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93322154-C-A

241209380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 93322154-C-T

241209386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 93322160-G-A

241209386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 93322160-G-T

241209433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93322207-G-A

241209433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93322207-G-T

http://identifiers.org/hco/2/GRCh38#241209434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93322208-C-A

241209434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93322208-C-T

241209472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93322240-G-A

241209472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93322240-G-T

http://identifiers.org/hco/2/GRCh38#241209474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93322247-C-A

241209509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 93322281-G-A

http://identifiers.org/hco/2/GRCh38#241209659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93322437-C-A

241209688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93322466-G-A

241209688-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93322466-G-C

241209688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93322466-G-T

241209885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93322632-G-A

241209959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93322692-C-G

http://identifiers.org/hco/2/GRCh38#241210116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93322884-C-A

241210117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93322885-A-G

http://identifiers.org/hco/2/GRCh38#241210146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93322896-C-A

241210146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93322896-C-T

http://identifiers.org/hco/2/GRCh38#241210174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93322921-C-A

http://identifiers.org/hco/2/GRCh38#241210177-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93322924-A-C

241210177-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93322924-A-T

241210237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93322961-G-T

241210442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93323161-G-A

241210442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93323161-G-T

241210453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93323172-C-T

241210458-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93323177-C-G

241210458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93323177-C-T

241212101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 93325006-C-T

241212188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 93325093-T-C

241212188-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93325093-T-G

241212241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93325146-C-G

241212268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93325169-G-A

241212268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93325169-G-T

241212297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93325179-G-A

241212297-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93325179-G-C

241212339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93325194-G-A

241212339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93325194-G-T

241212422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93325242-G-A

241212531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93325310-G-A

http://identifiers.org/hco/2/GRCh38#241212812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93325580-C-A

241212826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93325591-T-C

http://identifiers.org/hco/2/GRCh38#241212866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93325605-C-A

241213090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93325678-C-T

241213274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93325742-C-T

241213306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93325760-T-C

241213841-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93326202-C-G

http://identifiers.org/hco/2/GRCh38#241214685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93326683-C-A

241214685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93326683-C-T

http://identifiers.org/hco/2/GRCh38#241214697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93326695-C-A

241214773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 93326770-T-C

241214773-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 93326770-T-G

241214789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant, stop_lost
orthologous variants: 93326790-A-G

http://identifiers.org/hco/2/GRCh38#241214791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93326792-C-A

241214791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93326792-C-T

241214843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 93326845-G-A

http://identifiers.org/hco/2/GRCh38#241214917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93326919-C-A

241214917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93326919-C-T

http://identifiers.org/hco/2/GRCh38#241214939-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93326941-A-C

241214939-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93326941-A-T

241215430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93327331-T-C

http://identifiers.org/hco/2/GRCh38#241215468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93327348-C-A

241215468-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93327348-C-G

241215468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93327348-C-T

241215719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93327639-C-T

241216002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93328044-G-T

http://identifiers.org/hco/2/GRCh38#241216016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93328059-C-A

241217256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93328802-C-T

241217429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93328923-G-A

241217479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93328965-A-G

241217479-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93328965-A-T

241217501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93328989-G-A

241217501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93328989-G-T

http://identifiers.org/hco/2/GRCh38#241217680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93329147-C-A

241217680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 93329147-C-T

http://identifiers.org/hco/2/GRCh38#241217719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93329186-C-A

241217719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 93329186-C-T

http://identifiers.org/hco/2/GRCh38#241217720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#93329187-C-A

241217720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 93329187-C-T

http://identifiers.org/hco/2/GRCh38#241217732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#93329199-C-A

241217732-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 93329199-C-G

241217732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 93329199-C-T

241217737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 93329204-C-T

241218208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93329454-G-A

241218208-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93329454-G-C

241218208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93329454-G-T

241218230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93329474-G-A

241218230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93329474-G-T

http://identifiers.org/hco/2/GRCh38#241218241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#93329485-C-A

241218241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant, undefined
orthologous variants: 93329485-C-G

241218241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant, undefined
orthologous variants: 93329485-C-T

http://identifiers.org/hco/2/GRCh38#241218298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#93329542-C-A

241218298-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 93329542-C-G

241218298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 93329542-C-T

http://identifiers.org/hco/2/GRCh38#241218313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93329557-C-A

241218313-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 93329557-C-G

241218313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 93329557-C-T

http://identifiers.org/hco/2/GRCh38#241218361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#93329605-C-A

241218361-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 93329605-C-G

241218361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 93329605-C-T

241223261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 93329934-C-T

241223270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 93329943-G-A

241223356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_retained_variant, undefined
orthologous variants: 93330061-G-A

http://identifiers.org/hco/2/GRCh38#241223444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93330146-C-A

241223444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93330146-C-T

http://identifiers.org/hco/2/GRCh38#241223521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93330234-C-A

241223526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93330239-G-A

241223526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93330239-G-T

http://identifiers.org/hco/2/GRCh38#241223561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#93330271-C-A

241223561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93330271-C-T

http://identifiers.org/hco/2/GRCh38#241223592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93330289-C-A

241223592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93330289-C-T

241223631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93330337-G-A

241223631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93330337-G-T

http://identifiers.org/hco/2/GRCh38#241223685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93330386-C-A

241223716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 93330417-G-A

241223742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 93330443-G-A

241223742-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 93330443-G-C

241223850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93330592-C-T

241223884-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93330651-G-C

241223994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93330785-C-T

241224011-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93330823-C-G

241224011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93330823-C-T

http://identifiers.org/hco/2/GRCh38#241224207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93331075-C-A

241224207-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 93331075-C-G

241224207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 93331075-C-T

241224208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 93331076-G-A

241224208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 93331076-G-T

http://identifiers.org/hco/2/GRCh38#241227209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#93333592-C-A

241227210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31677
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 93333593-A-G