12991683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 3 prime UTR variant
orthologous variants: 64892822-A-G

12991717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 3 prime UTR variant
orthologous variants: 64892791-G-T

12991726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 3 prime UTR variant
orthologous variants: 64892782-T-C

12991729-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 3 prime UTR variant
orthologous variants: 64892779-C-G

12991778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 3 prime UTR variant
orthologous variants: 64892685-T-C

12991778-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 3 prime UTR variant
orthologous variants: 64892685-T-G

http://identifiers.org/hco/17/GRCh38#12991781-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64892682-A-C

12991805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 3 prime UTR variant
orthologous variants: 64892661-A-G

12991805-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 3 prime UTR variant
orthologous variants: 64892661-A-T

http://identifiers.org/hco/17/GRCh38#12992358-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64892431-A-C

12992464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 64892343-G-A

http://identifiers.org/hco/17/GRCh38#12992522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64892281-C-A

12992522-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 64892281-C-G

12992522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 64892281-C-T

http://identifiers.org/hco/17/GRCh38#12992536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64892271-C-A

12992536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 64892271-C-T

12992552-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 64892255-A-T

http://identifiers.org/hco/17/GRCh38#12992563-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64892244-A-C

12992563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 64892244-A-G

12992563-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 64892244-A-T

12992573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 64892241-T-C

12992573-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 64892241-T-G

12992577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 64892237-T-C

12992592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 64892218-G-A

12992592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 64892218-G-T

12992633-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 64892183-T-A

12992633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 64892183-T-C

12992644-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 64892179-T-A

12992644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 64892179-T-C

12992649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 64892174-A-G

12992649-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 64892174-A-T

http://identifiers.org/hco/17/GRCh38#12992672-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64892166-A-C

12992672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 64892166-A-G

12992672-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 64892166-A-T

http://identifiers.org/hco/17/GRCh38#12992979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64891885-C-A

12992979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 64891885-C-T

12993065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64891799-A-G

12993084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64891781-G-T

12993119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64891752-A-G

12993168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64891723-A-G

12993168-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64891723-A-T

http://identifiers.org/hco/17/GRCh38#12993175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64891716-C-A

12993300-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64891600-T-A

12993300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64891600-T-C

12993353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64891547-G-A

12993446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64891466-G-A

12993607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64891332-A-G

12993608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64891331-G-A

12993608-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64891331-G-C

12993608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64891331-G-T

12993671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64891281-C-T

12993774-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 64891177-C-G

12993802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 64891149-A-G

12993833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 64891118-T-C

12993833-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 64891118-T-G

12993912-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64891062-T-G

12993922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64891051-G-A

12993922-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64891051-G-C

12993941-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64891032-T-A

12993987-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64890993-A-T

12994145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64890860-C-T

12994178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64890844-T-C

12994192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64890830-G-A

12994261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64890766-A-G

12994276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64890751-G-T

12994279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64890748-C-T

12994327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64890702-G-T

12994514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64890500-A-G

12994542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64890475-C-T

12994543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64890474-G-A

http://identifiers.org/hco/17/GRCh38#12994715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64890310-C-A

12994746-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64890280-G-C

12994808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 64890218-A-G

12994838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 64890188-G-A

12994838-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 64890188-G-C

12994853-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 64890173-T-A

12994853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 64890173-T-C

12994893-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64890133-G-C

12994953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64890070-T-C

http://identifiers.org/hco/17/GRCh38#12994985-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64890038-A-C

12995063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 64889960-C-T

12995216-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64889812-A-T

12995614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64889529-T-C

12995614-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64889529-T-G

http://identifiers.org/hco/17/GRCh38#12995662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64889483-C-A

http://identifiers.org/hco/17/GRCh38#12995686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64889458-C-A

12995686-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64889458-C-G

http://identifiers.org/hco/17/GRCh38#12995784-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64889360-A-C

12995784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 64889360-A-G

12995826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64889319-T-C

http://identifiers.org/hco/17/GRCh38#12995828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64889317-C-A

12995828-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64889317-C-G

12995828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64889317-C-T

12995856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64889290-C-T

12995971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 64889172-G-A

12995971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 64889172-G-T

12996012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64889134-G-A

12996012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64889134-G-T

12996074-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64889075-C-G

http://identifiers.org/hco/17/GRCh38#12996091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64889067-C-A

12996091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64889067-C-T

12996111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64889054-G-T

http://identifiers.org/hco/17/GRCh38#12996190-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64889002-A-C

12996190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64889002-A-G

12996220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64888971-G-A

12996220-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64888971-G-C

12996277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64888945-G-A

12996277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64888945-G-T

12996279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64888943-G-A

12996279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64888943-G-T

12996584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 64888793-G-C

12996674-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 64888703-G-C

12996674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 64888703-G-T

12996718-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64888672-A-T

12996720-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64888670-T-G

http://identifiers.org/hco/17/GRCh38#12996740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64888650-C-A

12996747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64888643-T-C

12996756-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64888634-C-G

12996756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64888634-C-T

12996793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64888586-G-A

12996793-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64888586-G-C

12996793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64888586-G-T

12996817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64888558-G-A

12996817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64888558-G-T

12996878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64888496-T-C

12997013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64888377-T-C

12997176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64888246-G-A

12997176-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64888246-G-C

12997254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64888191-G-T

12997258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64888187-T-C

12997343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64888129-G-A

12998474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 64886164-A-G

12998534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64886103-T-C

http://identifiers.org/hco/17/GRCh38#12998549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64886090-C-A

13000179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 64885155-G-A

13000179-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 64885155-G-C

http://identifiers.org/hco/17/GRCh38#13000259-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64885075-A-C

13000298-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64885042-T-G

13001597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 64883813-T-C

13002176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 64883445-G-T

13002197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 64883424-C-T

13002250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 64883372-C-T

13002261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 64883361-A-G

13002336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 64883286-C-T

13002342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 64883280-G-A

13002409-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64883215-T-G

13002446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 64883178-A-G

13002488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 64883136-G-A

13002488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 64883136-G-C

13002490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 64883134-T-C

13002568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 64883056-T-C

13002599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64883026-G-A

13002599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64883026-G-T

http://identifiers.org/hco/17/GRCh38#13002630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64882996-C-A

13002639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64882987-G-A

13002639-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64882987-G-C

13002639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64882987-G-T

http://identifiers.org/hco/17/GRCh38#13002688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64882939-C-A

13002757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 64882874-G-T

13002784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 64882860-G-A

13002784-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 64882860-G-C

13002784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 64882860-G-T

13002798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 64882846-G-A

13002798-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 64882846-G-C

13002798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 64882846-G-T

13002820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 64882822-G-T

13002822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 64882820-A-G

13002822-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 64882820-A-T

13002837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 64882801-A-G

13003391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 64880367-A-G

13003431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 64880328-C-T

13003502-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 64880249-G-C

13003505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 64880246-G-A

13003505-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 64880246-G-C

13003564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 64880187-T-C

http://identifiers.org/hco/17/GRCh38#13003599-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64880144-A-C

13003615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64880128-A-G

13003637-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64880106-A-T

13004641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64879382-T-C

13004773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64879233-G-A

http://identifiers.org/hco/17/GRCh38#13004979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64878978-C-A

13004979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64878978-C-T

13005001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 64878956-G-A

http://identifiers.org/hco/17/GRCh38#13005026-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64878931-A-C

13005075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 64878882-A-G

13005121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64878837-C-T

http://identifiers.org/hco/17/GRCh38#13005190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64878767-C-A

13005190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64878767-C-T

http://identifiers.org/hco/17/GRCh38#13005191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64878766-C-A

13005191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64878766-C-T

13005351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64878639-C-T

13005476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64878556-A-G

13005526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64878531-G-A

13005561-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64878491-G-C

13005668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64878389-T-C

13005668-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64878389-T-G

13005688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64878370-C-T

13005875-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64878191-C-G

13005875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64878191-C-T

13005990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64878084-G-A

13010488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64876585-G-T

13010495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64876578-T-C

http://identifiers.org/hco/17/GRCh38#13010517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64876556-C-A

13010548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64876527-G-A

13010548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64876527-G-T

http://identifiers.org/hco/17/GRCh38#13010582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64876482-C-A

13010582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64876482-C-T

http://identifiers.org/hco/17/GRCh38#13010601-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64876463-A-C

13010601-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64876463-A-T

13010683-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64876375-C-G

13010683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64876375-C-T

13010706-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64876358-A-T

13011701-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 64874499-T-A

13011785-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 64874415-G-C

13012130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64874127-A-G

13012207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64874036-C-T

13012254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64873991-C-T

13013126-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64873732-T-A

13013132-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64873726-G-C

13013132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64873726-G-T

http://identifiers.org/hco/17/GRCh38#13013144-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64873714-A-C

13013150-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64873708-G-C

13013171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64873687-C-T

13013281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 64873574-A-G

13013302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64873553-G-A

13013306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64873549-T-C

13013351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64873519-A-G

http://identifiers.org/hco/17/GRCh38#13013352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64873518-C-A

13013363-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64873511-T-A

13013367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64873507-T-C

13013367-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64873507-T-G

http://identifiers.org/hco/17/GRCh38#13013380-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64873494-A-C

13013385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64873489-G-A

13013406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64873468-G-A

13013573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64873303-A-G

13013726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64873110-G-A

13013773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64873065-G-T

13013828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64873024-C-T

13013922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64872925-T-C

13014332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64872605-T-C

13014332-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64872605-T-G

http://identifiers.org/hco/17/GRCh38#13014342-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64872595-A-C

13014342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64872595-A-G

13014342-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64872595-A-T

13014377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64872558-T-C

http://identifiers.org/hco/17/GRCh38#13014385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64872551-C-A

13014401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64872536-T-C

13014524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64872420-T-C

13014608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64872345-A-G

13014636-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64872318-T-A

13014835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64872142-C-T

http://identifiers.org/hco/17/GRCh38#13015021-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64872051-A-C

13015021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64872051-A-G

13015024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64872048-G-A

13015024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64872048-G-T

13015103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64871981-G-A

13015130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64871954-T-C

13015154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64871939-T-C

13015406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64871828-C-T

13015475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64871769-A-G

13015686-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64871568-T-A

13015686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64871568-T-C

13015709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64871548-T-C

13015712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64871545-T-C

http://identifiers.org/hco/17/GRCh38#13015823-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64871441-A-C

13015829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 64871435-A-G

13015861-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64871394-T-A

13015886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64871366-A-G

13016426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64870973-T-C

13016440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64870959-C-T

13016486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64870914-G-A

13016486-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64870914-G-C

http://identifiers.org/hco/17/GRCh38#13016497-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64870903-A-C

http://identifiers.org/hco/17/GRCh38#13016815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64870846-C-A

13016845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64870817-G-A

13016960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64870702-A-G

13016967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64870695-G-A

13016967-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64870695-G-C

13016967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64870695-G-T

http://identifiers.org/hco/17/GRCh38#13017055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64870607-C-A

13017055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64870607-C-T

13017298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64870419-G-A

13017298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64870419-G-C

13017298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64870419-G-T

13017473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64870299-G-A

13017473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64870299-G-T

13017474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64870298-G-A

13017474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64870298-G-T

13017476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64870296-T-C

13017476-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64870296-T-G

13017601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 64870233-A-G

13017601-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 64870233-A-T

13017602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 64870232-T-C

13017602-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 64870232-T-G

13017737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 64870121-C-T

13017823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 64870041-G-A

13017823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 64870041-G-C

13017835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 64870029-C-T

13017849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 64870015-G-A

http://identifiers.org/hco/17/GRCh38#13017850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#64870014-C-A

13017850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 64870014-C-T

http://identifiers.org/hco/17/GRCh38#13017862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#64870002-C-A

13017862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 64870002-C-T

13017892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, missense_variant
orthologous variants: 64869990-C-T

13017909-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 64869973-T-A

13017909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 64869973-T-C

13017910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 64869972-C-T

13017925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, missense_variant
orthologous variants: 64869957-A-G

13017928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, missense_variant
orthologous variants: 64869954-A-G

13017932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: intron_variant, missense_variant
orthologous variants: 64869950-A-G

http://identifiers.org/hco/17/GRCh38#13018057-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64869832-A-C

13018057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 5 prime UTR variant
orthologous variants: 64869832-A-G

13018060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 64869829-G-A

13018060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14198
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 64869829-G-T