50110114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94917989-G-A

50110114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94917989-G-T

http://identifiers.org/hco/17/GRCh38#50110134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94917972-C-A

50110134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94917972-C-T

50110178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94917925-G-A

50110178-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94917925-G-C

50110178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94917925-G-T

http://identifiers.org/hco/17/GRCh38#50110299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94917803-C-A

50110332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3 prime UTR variant
orthologous variants: 94917763-G-A

50110332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3 prime UTR variant
orthologous variants: 94917763-G-T

50110407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3 prime UTR variant
orthologous variants: 94917706-C-T

http://identifiers.org/hco/17/GRCh38#50110655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94917444-C-A

50110655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3 prime UTR variant
orthologous variants: 94917444-C-T

http://identifiers.org/hco/17/GRCh38#50110800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94917327-C-A

50110800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3 prime UTR variant
orthologous variants: 94917327-C-T

50110836-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3 prime UTR variant
orthologous variants: 94917293-G-C

50110892-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3 prime UTR variant
orthologous variants: 94917237-C-G

50110967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3 prime UTR variant
orthologous variants: 94917164-A-G

50111070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3 prime UTR variant
orthologous variants: 94917069-T-C

50111070-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3 prime UTR variant
orthologous variants: 94917069-T-G

http://identifiers.org/hco/17/GRCh38#50111159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94916991-C-A

50111159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3 prime UTR variant
orthologous variants: 94916991-C-T

50111179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3 prime UTR variant
orthologous variants: 94916980-G-A

50111183-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3 prime UTR variant
orthologous variants: 94916976-A-T

50111216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3 prime UTR variant
orthologous variants: 94916949-C-T

50111353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94916877-G-T

http://identifiers.org/hco/17/GRCh38#50111471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94916771-C-A

50111471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94916771-C-T

http://identifiers.org/hco/17/GRCh38#50111496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94916743-C-A

http://identifiers.org/hco/17/GRCh38#50111515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94916723-C-A

50111515-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94916723-C-G

50111515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94916723-C-T

50111537-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94916719-T-A

50111537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94916719-T-C

50111615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94916644-C-T

50111658-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94916608-G-C

50111658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94916608-G-T

50111674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94916595-C-T

http://identifiers.org/hco/17/GRCh38#50111826-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94916482-A-C

50111826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94916482-A-G

http://identifiers.org/hco/17/GRCh38#50111859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94916449-C-A

50111859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94916449-C-T

50111875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94916430-T-C

50111884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94916421-T-C

50111963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94916345-G-A

50111963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94916345-G-T

50112095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94916251-T-C

50112172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94916205-G-T

50112222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94916170-G-A

50112226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94916166-G-A

50112239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94916153-G-A

50112240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94916152-G-A

50112240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94916152-G-T

50112263-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94916122-A-T

http://identifiers.org/hco/17/GRCh38#50112284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94916102-C-A

50112284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94916102-C-T

50112418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94915980-G-T

50112446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94915953-C-T

50112604-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94915804-T-A

50112604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94915804-T-C

http://identifiers.org/hco/17/GRCh38#50112646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94915764-C-A

50112646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94915764-C-T

http://identifiers.org/hco/17/GRCh38#50112699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94915711-C-A

50112749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94915671-A-G

50112758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94915662-G-A

50112758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94915662-G-T

50112814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94915628-G-A

50112814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94915628-G-T

50112829-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94915613-T-A

50112834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94915608-C-T

http://identifiers.org/hco/17/GRCh38#50112865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94915586-C-A

50112865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94915586-C-T

50112911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 94915539-C-T

50112945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94915505-G-A

50112957-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94915493-T-A

50112957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94915493-T-C

50113178-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94915315-C-G

50113178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94915315-C-T

50113199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94915313-A-G

http://identifiers.org/hco/17/GRCh38#50113210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94915302-C-A

50113244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94915268-G-A

50113244-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94915268-G-C

50113244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94915268-G-T

http://identifiers.org/hco/17/GRCh38#50113291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94915218-C-A

50113325-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94915184-G-C

50113325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94915184-G-T

http://identifiers.org/hco/17/GRCh38#50113370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94915139-C-A

http://identifiers.org/hco/17/GRCh38#50113389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94915120-C-A

50113389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94915120-C-T

http://identifiers.org/hco/17/GRCh38#50113402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94915107-C-A

50113402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94915107-C-T

50113660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94914696-T-C

50113781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94914582-G-T

50114116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94914251-G-A

http://identifiers.org/hco/17/GRCh38#50114117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94914250-C-A

50114117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94914250-C-T

50114171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94914218-G-A

50114251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94914138-C-T

50114321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94914068-G-T

50114327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94914062-G-A

50114332-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94914058-T-G

50114487-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94913896-C-G

50114522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94913862-G-T

http://identifiers.org/hco/17/GRCh38#50114575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94913808-C-A

50114575-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94913808-C-G

50114575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94913808-C-T

http://identifiers.org/hco/17/GRCh38#50114577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94913806-C-A

50114577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94913806-C-T

50114611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94913768-C-T

50114727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94913457-G-A

50114727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94913457-G-T

50114758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94913425-A-G

50114780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94913401-G-A

50114780-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94913401-G-C

50114810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94913364-A-G

http://identifiers.org/hco/17/GRCh38#50114928-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#94913305-A-C

50114928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 94913305-A-G

50114945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 94913288-G-A

50114945-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 94913288-G-C

50115159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94913108-T-C

50115446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94912829-A-G

50115486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94912788-C-T

http://identifiers.org/hco/17/GRCh38#50115533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#94912745-C-A

50115533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94912745-C-T

50115808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94912313-G-A

50115809-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94912312-G-C

50115809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94912312-G-T

http://identifiers.org/hco/17/GRCh38#50115868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94912246-C-A

50116155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94911957-G-A

50116157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94911955-G-A

50116157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94911955-G-T

50116205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94911911-G-A

50116205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94911911-G-T

http://identifiers.org/hco/17/GRCh38#50116396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94911760-C-A

50116396-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94911760-C-G

50116396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94911760-C-T

50116443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94911714-T-C

http://identifiers.org/hco/17/GRCh38#50116506-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94911662-A-C

50116506-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94911662-A-T

50116627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94911531-G-A

http://identifiers.org/hco/17/GRCh38#50117291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#94911121-C-A

50117292-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94911120-T-A

50117292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94911120-T-C

50117299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94911113-G-A

50117299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94911113-G-T

50117416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 94911033-G-A

50117416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 94911033-G-T

50117433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 94911016-T-C

http://identifiers.org/hco/17/GRCh38#50117457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#94910992-C-A

50117457-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 94910992-C-G

50117457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 94910992-C-T

50117496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94910953-G-A

50117496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94910953-G-T

50117499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94910950-G-A

50117499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94910950-G-T

http://identifiers.org/hco/17/GRCh38#50117595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94910854-C-A

50117595-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94910854-C-G

50117595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94910854-C-T

50117684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 94910765-G-A

50117684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 94910765-G-T

50117702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 94910747-G-A

50117702-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 94910747-G-C

50117702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 94910747-G-T

http://identifiers.org/hco/17/GRCh38#50117766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#94910691-C-A

http://identifiers.org/hco/17/GRCh38#50117767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#94910690-C-A

http://identifiers.org/hco/17/GRCh38#50117903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94910565-C-A

50117903-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94910565-C-G

50117903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94910565-C-T

50117977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94910501-A-G

50117977-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94910501-A-T

50118065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94910423-G-A

50118065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94910423-G-T

50118195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94910317-T-C

50118421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94910141-A-G

50118558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94910035-A-G

http://identifiers.org/hco/17/GRCh38#50118621-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94909966-A-C

50118963-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94909651-G-C

50118963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94909651-G-T

http://identifiers.org/hco/17/GRCh38#50119130-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94909529-A-C

50119205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94909428-C-T

50119218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94909415-T-C

http://identifiers.org/hco/17/GRCh38#50119501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94909151-C-A

50119527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94909126-T-C

50119749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94908899-T-C

50120156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94908480-G-A

50120379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94908313-G-A

50120849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94908054-C-T

50123412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94906962-G-A

50123436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94906938-G-T

50123548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94906849-G-T

http://identifiers.org/hco/17/GRCh38#50123554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94906843-C-A

50123554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94906843-C-T

50123558-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94906839-A-T

50123561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94906836-G-A

50123561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94906836-G-T

50123586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94906812-G-A

50123586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94906812-G-T

50123590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94906808-A-G

http://identifiers.org/hco/17/GRCh38#50123593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94906805-C-A

50123601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94906797-G-T

http://identifiers.org/hco/17/GRCh38#50123646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94906785-C-A

50123646-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94906785-C-G

http://identifiers.org/hco/17/GRCh38#50123670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94906764-C-A

50123670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94906764-C-T

50123689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94906749-T-C

http://identifiers.org/hco/17/GRCh38#50123723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94906728-C-A

50123765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94906682-C-T

50124017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94906390-G-T

50124038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94906363-G-A

50124063-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94906329-C-G

50124063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94906329-C-T

http://identifiers.org/hco/17/GRCh38#50124133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#94906309-C-A

50124208-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 94906225-T-G

http://identifiers.org/hco/17/GRCh38#50124825-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94905329-A-C

50124825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94905329-A-G

50124842-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94905310-A-T

50125192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94905003-G-A

50125192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94905003-G-C

50125192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94905003-G-T

http://identifiers.org/hco/17/GRCh38#50125347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94904869-C-A

50125378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94904840-G-T

50125450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94904772-A-G

50126063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94903923-G-A

50126096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94903896-T-C

50127842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94903302-C-T

http://identifiers.org/hco/17/GRCh38#50127896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94903249-C-A

50128114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94903079-C-T

50128129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94903064-T-C

http://identifiers.org/hco/17/GRCh38#50128161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94903033-C-A

http://identifiers.org/hco/17/GRCh38#50128438-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94902744-A-C

50128549-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94902677-T-G

50128554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94902672-C-T

50129452-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94901465-C-G

50129452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94901465-C-T

50129583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94901334-G-T

50129604-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94901313-T-G

50129841-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 5 prime UTR variant
orthologous variants: 94901064-T-A

50129841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 5 prime UTR variant
orthologous variants: 94901064-T-C

http://identifiers.org/hco/17/GRCh38#50129881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#94901012-C-A

http://identifiers.org/hco/17/GRCh38#50129888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#94901005-C-A

50129888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27312
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 94901005-C-T