175157078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159906525-T-C

175157090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159906513-C-T

175157107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159906496-A-G

175157153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159906461-C-T

175157301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159906348-G-A

175157304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159906345-G-A

175157345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159906308-G-A

175157382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159906272-G-T

175157409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159906251-G-A

175157410-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159906250-G-C

175157410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159906250-G-T

175157487-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159906206-G-C

175157487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159906206-G-T

175157508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159906184-G-A

175157522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159906167-C-T

175157686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159905996-G-A

175157686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159905996-G-T

http://identifiers.org/hco/1/GRCh38#175157689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159905993-C-A

175157689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159905993-C-T

http://identifiers.org/hco/1/GRCh38#175157705-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159905977-A-C

175157778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159905925-G-A

175157799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159905904-A-G

175157799-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159905904-A-T

175157808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159905893-G-T

http://identifiers.org/hco/1/GRCh38#175157900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159905644-C-A

http://identifiers.org/hco/1/GRCh38#175157910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159905634-C-A

175157930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159905608-G-A

175157930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159905608-G-T

175157933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159905604-G-A

175157933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159905604-G-T

http://identifiers.org/hco/1/GRCh38#175157934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159905603-C-A

175157934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159905603-C-T

175157957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159905579-G-T

175157975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159905563-G-T

175158071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159905487-G-A

175158071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159905487-G-T

175158148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159905424-C-T

175158152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159905420-A-G

175158171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159905395-C-T

175158186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159905381-T-C

http://identifiers.org/hco/1/GRCh38#175158224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159905347-C-A

175158225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159905346-T-C

http://identifiers.org/hco/1/GRCh38#175158278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159905302-C-A

175158283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159905297-T-C

175158359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159905220-T-C

175158446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159905129-C-T

175158449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159905126-G-A

175158552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159905025-A-G

175158773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159904842-G-A

175158773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159904842-G-T

175158787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159904828-G-A

175158787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159904828-G-T

175158936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159904726-C-T

175158946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159904716-G-A

175158946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159904716-G-T

175158954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159904708-A-G

175159250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159904434-A-G

175159257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159904427-T-C

http://identifiers.org/hco/1/GRCh38#175159395-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159904305-A-C

175159395-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159904305-A-T

http://identifiers.org/hco/1/GRCh38#175159650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159904022-C-A

175159650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159904022-C-T

175159679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159903992-T-C

175159824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159903841-G-A

175159931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159903738-G-T

175159999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159903677-T-C

175160005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159903671-C-T

http://identifiers.org/hco/1/GRCh38#175160049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159903622-C-A

http://identifiers.org/hco/1/GRCh38#175160076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159903595-C-A

175160076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159903595-C-T

175160078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159903593-G-T

175160080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3 prime UTR variant
orthologous variants: 159903591-T-C

175160203-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 159903483-T-G

175160219-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 159903467-A-T

175160249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 159903437-G-A

http://identifiers.org/hco/1/GRCh38#175160308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159903386-C-A

175160308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3_prime_UTR_variant, stop_gained
orthologous variants: 159903386-C-T

http://identifiers.org/hco/1/GRCh38#175160495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159903226-C-A

175160495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 159903226-C-T

http://identifiers.org/hco/1/GRCh38#175160539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159903184-C-A

175160539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 159903184-C-T

175160591-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 159903139-T-G

175160619-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 159903115-G-C

175160619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 159903115-G-T

175160642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant
orthologous variants: 159903097-T-C

175160695-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant
orthologous variants: 159903047-A-T

175160839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 159902904-C-T

http://identifiers.org/hco/1/GRCh38#175161110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159902635-C-A

175161110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 159902635-C-T

http://identifiers.org/hco/1/GRCh38#175161141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159902604-C-A

175161141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 159902604-C-T

175161241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159902504-G-A

175161271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159902474-T-C

175161866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159902013-C-T

175162365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159901587-T-C

175162713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159901211-G-T

http://identifiers.org/hco/1/GRCh38#175162826-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159901106-A-C

175162826-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159901106-A-T

175163457-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159900505-C-G

http://identifiers.org/hco/1/GRCh38#175163483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159900479-C-A

175163577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159900373-T-C

175163692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159900265-G-A

175163765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159900163-A-G

175163839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159900108-A-G

175164253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159899773-C-T

http://identifiers.org/hco/1/GRCh38#175164420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159899610-C-A

175164490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159899540-A-G

http://identifiers.org/hco/1/GRCh38#175164505-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159899525-A-C

175165113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159898930-C-T

175165167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159898875-G-T

175165178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159898864-C-T

175165196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159898846-G-A

175165265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159898783-C-T

175165326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159898727-C-T

175165511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159896305-C-T

http://identifiers.org/hco/1/GRCh38#175165731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159896090-C-A

175167719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159895809-G-A

175168059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159895506-C-T

175168111-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159895457-A-T

http://identifiers.org/hco/1/GRCh38#175170722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159893449-C-A

175170945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159893190-C-T

175170960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159893155-G-T

175171301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159892773-T-C

http://identifiers.org/hco/1/GRCh38#175171605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159892443-C-A

175172049-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159892004-C-G

175172120-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159891933-A-T

175172142-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159891912-G-C

175172981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159891386-T-C

175173067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159891300-T-C

175173188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159891179-T-C

175173201-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159891165-C-G

175173736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159889559-C-T

175174104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159889211-G-A

http://identifiers.org/hco/1/GRCh38#175174233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159889087-C-A

175174303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159889024-G-A

175174304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159889023-G-A

175174374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159888954-C-T

http://identifiers.org/hco/1/GRCh38#175174509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159888771-C-A

175174509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159888771-C-T

175174673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159888611-T-C

175174673-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159888611-T-G

175174752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159888526-C-T

http://identifiers.org/hco/1/GRCh38#175174793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159888494-C-A

175175181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159888139-G-A

175175186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159888134-C-T

175175200-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159888120-T-G

175175216-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159888104-C-G

175175216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159888104-C-T

175176401-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 159887735-T-G

175176427-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 159887706-T-A

http://identifiers.org/hco/1/GRCh38#175176541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159887633-C-A

175176766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159887421-T-C

175176862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159887339-G-A

175176862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159887339-G-T

175177122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159886784-G-T

175177309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159886597-A-G

175177445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159886467-T-C

175177533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159886371-G-A

175177543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159886362-T-C

175177587-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159886320-G-C

175177587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159886320-G-T

175177596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159886311-G-A

175177596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159886311-G-T

175177624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 159886284-T-C

175177709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159886201-T-C

175177709-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159886201-T-G

175177744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159886166-C-T

http://identifiers.org/hco/1/GRCh38#175177772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159886149-C-A

175177797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159886122-T-C

175177924-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159885885-A-T

175178354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159885345-G-T

175178586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159885118-G-A

175178712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159884995-G-A

175178875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159884359-T-C

175178981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159884278-A-G

175178981-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159884278-A-T

175179456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159883859-T-C

175179456-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159883859-T-G

175179518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159883798-A-G

175179942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159883273-A-G

175180240-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159882972-C-G

175180246-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159882966-T-G

175180409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159882817-C-T

175180581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159882650-A-G

175180582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159882649-T-C

http://identifiers.org/hco/1/GRCh38#175180622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159882609-C-A

175180760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159882547-T-C

175181614-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159882013-T-A

http://identifiers.org/hco/1/GRCh38#175181852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159881787-C-A

http://identifiers.org/hco/1/GRCh38#175181919-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159881721-A-C

175181919-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159881721-A-T

175181965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159881677-G-A

175182062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159881582-G-A

175182155-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 159881499-T-A

175182620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159880646-C-T

175182725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159880527-T-C

175183058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159880212-T-C

175183118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159880161-G-A

175183179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159880091-G-A

http://identifiers.org/hco/1/GRCh38#175183262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159880023-C-A

175183262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159880023-C-T

175183341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159879937-G-A

175183395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159879883-T-C

175183642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159879694-G-A

http://identifiers.org/hco/1/GRCh38#175183725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159879614-C-A

http://identifiers.org/hco/1/GRCh38#175185440-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159878880-A-C

175185497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159878829-T-C

175185669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159878663-C-G

175185669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159878663-C-T

175185880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159878450-A-G

175186067-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159878290-T-A

175186067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159878290-T-C

175186234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159878135-T-C

175186410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159878004-C-T

175186656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159877795-C-T

175186910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159877542-A-G

http://identifiers.org/hco/1/GRCh38#175187266-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159877181-A-C

175187370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159877086-C-T

175188193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159876289-C-T

175188639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159875847-C-T

175188692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159875786-G-A

175188692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159875786-G-T

175188909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159875589-T-C

175188909-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159875589-T-G

175189092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 159875405-G-A

175189203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159875337-T-C

175189358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159875165-C-G

175189358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159875165-C-T

175189368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159875155-G-A

175189388-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159875135-G-C

175189388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159875135-G-T

175189506-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159875015-A-T

175189616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159874896-G-A

175189860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159874667-T-C

175190863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159874077-A-G

http://identifiers.org/hco/1/GRCh38#175190989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159873958-C-A

175191311-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159873671-T-A

175191646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159873287-C-T

175191834-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159873119-C-G

175191834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159873119-C-T

175192014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159872945-C-T

175192212-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159872765-T-G

175192271-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159872678-T-A

175192362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159872592-G-T

175192426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159872522-G-A

175192496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159872471-A-G

175192513-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159872454-T-A

175192568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 159872404-G-T

175192649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 159872312-C-T

175192652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 159872309-G-A

175192689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 159872278-G-A

175192689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 159872278-G-T

175192731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 159872233-G-A

175192731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 159872233-G-T

http://identifiers.org/hco/1/GRCh38#175192754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159872213-C-A

175192754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 159872213-C-T

175192869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 159872150-C-T

175192949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 159872099-G-T

175192970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 159872078-G-A

175192970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28950
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 159872078-G-T